A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696842



Internal ID15433494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155359727..155376109hg38UCSC Ensembl
Innerchr6:155680861..155697243hg19UCSC Ensembl
Innerchr6:155722553..155738935hg18UCSC Ensembl
Innerchr6:155772974..155789356hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3816383
hg1916383
hg1816383
hg1716383
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520490
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696842
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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