A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016441



Internal ID19105660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47057928..47089824hg38UCSC Ensembl
Innerchr7:47097526..47129422hg19UCSC Ensembl
Innerchr7:47064051..47095947hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3831897
hg1931897
hg1831897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6343n100
Supporting Variantsnssv3661236
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)nsv1016441
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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