A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659799



Internal ID15396451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149090068..149092197hg38UCSC Ensembl
Innerchr2:149946582..149948711hg19UCSC Ensembl
Innerchr2:149654828..149656957hg18UCSC Ensembl
Innerchr2:149772090..149774219hg17UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg382130
hg192130
hg182130
hg172130
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515662
Supporting Variants
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659799
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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