A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697780



Internal ID15434432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4904703..4907636hg38UCSC Ensembl
Innerchr11:4925933..4928866hg19UCSC Ensembl
Innerchr11:4882509..4885442hg18UCSC Ensembl
Innerchr11:4882509..4885442hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382934
hg192934
hg182934
hg172934
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521088
Supporting Variants
Samples
Known GenesOR51A7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697780
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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