A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033757



Internal ID19122978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25432603..25464802hg38UCSC Ensembl
Innerchr7:25472222..25504421hg19UCSC Ensembl
Innerchr7:25438747..25470946hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3832200
hg1932200
hg1832200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6308n100
Supporting Variantsnssv3643309, nssv3643308
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)nsv1033757
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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