A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672719



Internal ID15062685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72578056..72812986hg38UCSC Ensembl
Innerchr7:72043041..72283565hg19UCSC Ensembl
Innerchr7:71680977..71921501hg18UCSC Ensembl
Innerchr7:71487692..71728216hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38234931
hg19240525
hg18240525
hg17240525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520573
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, TYW1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672719
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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