A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697489



Internal ID15087455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:219177514..219194620hg38UCSC Ensembl
Innerchr1:219350856..219367962hg19UCSC Ensembl
Innerchr1:217417479..217434585hg18UCSC Ensembl
Innerchr1:215739251..215756357hg17UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3817107
hg1917107
hg1817107
hg1717107
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520564
Supporting Variants
Samples
Known GenesLYPLAL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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