A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032992



Internal ID18775526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1063632..1263413hg38UCSC Ensembl
Innerchr7:1103268..1303049hg19UCSC Ensembl
Innerchr7:1069794..1269575hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38199782
hg19199782
hg18199782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752787
Samples
Known GenesC7orf50, GPER1, UNCX, ZFAND2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032992
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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