A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699095



Internal ID15089061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30914736..30926164hg38UCSC Ensembl
Innerchr6:30882513..30893941hg19UCSC Ensembl
Innerchr6:30990492..31001920hg18UCSC Ensembl
Innerchr6:30990492..31001920hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3811429
hg1911429
hg1811429
hg1711429
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523346
Supporting Variants
Samples
Known GenesVARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699095
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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