A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705040



Internal ID15095006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18252544..18274330hg38UCSC Ensembl
Innerchr1:18579038..18600824hg19UCSC Ensembl
Innerchr1:18451625..18473411hg18UCSC Ensembl
Innerchr1:18324344..18346130hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821787
hg1921787
hg1821787
hg1721787
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528445
Supporting Variants
Samples
Known GenesIGSF21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705040
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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