A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023637



Internal ID19112854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52646339..52675038hg38UCSC Ensembl
Innerchr7:52714035..52742733hg19UCSC Ensembl
Innerchr7:52681529..52710227hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3828700
hg1928699
hg1828699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661277
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)nsv1023637
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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