A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642982



Internal ID18941263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12503535..12580115hg38UCSC Ensembl
Innerchr7:12543161..12619740hg19UCSC Ensembl
Innerchr7:12509686..12586265hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3876581
hg1976580
hg1876580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027831
Supporting Variants
Samples
Known GenesSCIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642982
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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