A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436941



Internal ID15383182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68562504..68572597hg38UCSC Ensembl
Outerchr4:68559473..68577376hg38UCSC Ensembl
Innerchr4:69428222..69438315hg19UCSC Ensembl
Outerchr4:69425191..69443094hg19UCSC Ensembl
Innerchr4:69110817..69120910hg18UCSC Ensembl
Outerchr4:69107786..69125689hg18UCSC Ensembl
Innerchr4:69431602..69441695hg16UCSC Ensembl
Outerchr4:69428571..69446474hg16UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3817904
hg1917904
hg1817904
hg1617904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466822
SamplesNA10846
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)nsv436941
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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