A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437403



Internal ID15036135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87834835..87834958hg38UCSC Ensembl
Outerchr4:87833529..87849846hg38UCSC Ensembl
Innerchr4:88755987..88756110hg19UCSC Ensembl
Outerchr4:88754681..88770998hg19UCSC Ensembl
Innerchr4:88975011..88975134hg18UCSC Ensembl
Outerchr4:88973705..88990022hg18UCSC Ensembl
Innerchr4:89214382..89214505hg16UCSC Ensembl
Outerchr4:89213076..89229393hg16UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3816318
hg1916318
hg1816318
hg1616318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv94n17
Supporting Variantsnssv467284
SamplesNA19142
Known GenesMEPE
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)nsv437403
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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