A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436942



Internal ID15035758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68572597..68589392hg38UCSC Ensembl
Outerchr4:68559473..68593441hg38UCSC Ensembl
Innerchr4:69438315..69455110hg19UCSC Ensembl
Outerchr4:69425191..69459159hg19UCSC Ensembl
Innerchr4:69120910..69137705hg18UCSC Ensembl
Outerchr4:69107786..69141754hg18UCSC Ensembl
Innerchr4:69441695..69458490hg16UCSC Ensembl
Outerchr4:69428571..69462539hg16UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3833969
hg1933969
hg1833969
hg1633969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n17
Supporting Variantsnssv466823
SamplesNA10857
Known GenesUGT2B17
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv436942
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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