A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981438



Internal ID18616635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22527358..22542089hg38UCSC Ensembl
Innerchr7:22566977..22581708hg19UCSC Ensembl
Innerchr7:22533502..22548233hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3814732
hg1914732
hg1814732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438447, nssv2438446, nssv2438445, nssv2438438, nssv2438441, nssv2438443, nssv2438444, nssv2438439, nssv2438440, nssv2438442
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981438
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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