A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683032



Internal ID15072998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57140959..57530097hg38UCSC Ensembl
Innerchr7:57208666..57589803hg19UCSC Ensembl
Innerchr7:57212608..57593745hg18UCSC Ensembl
Innerchr7:57019323..57400460hg17UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38389139
hg19381138
hg18381138
hg17381138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520659
Supporting Variants
Samples
Known GenesGUSBP10, MIR3147, ZNF716
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683032
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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