A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643122



Internal ID18941403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13090444..13326153hg38UCSC Ensembl
Innerchr7:13130069..13365778hg19UCSC Ensembl
Innerchr7:13096594..13332303hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38235710
hg19235710
hg18235710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643122
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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