A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642980



Internal ID18941261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12503535..12572434hg38UCSC Ensembl
Innerchr7:12543161..12612059hg19UCSC Ensembl
Innerchr7:12509686..12578584hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3868900
hg1968899
hg1868899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025397
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)nssv3642980
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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