A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660656



Internal ID15050622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144000454..144135334hg38UCSC Ensembl
Innerchr4:144921607..145056487hg19UCSC Ensembl
Innerchr4:145141057..145275937hg18UCSC Ensembl
Innerchr4:145279212..145414092hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38134881
hg19134881
hg18134881
hg17134881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517006
Supporting Variants
Samples
Known GenesGYPA, GYPB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660656
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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