A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034074



Internal ID19123296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1263385..1337400hg38UCSC Ensembl
Innerchr7:1303021..1377036hg19UCSC Ensembl
Innerchr7:1269547..1343562hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3874016
hg1974016
hg1874016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654222
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)nsv1034074
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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