A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660854



Internal ID15397506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129271481..129375670hg38UCSC Ensembl
Innerchr7:128911322..129015511hg19UCSC Ensembl
Innerchr7:128698558..128802747hg18UCSC Ensembl
Innerchr7:128505273..128609462hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38104190
hg19104190
hg18104190
hg17104190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516498
Supporting Variants
Samples
Known GenesAHCYL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660854
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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