A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981437



Internal ID18616634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21245197..21247432hg38UCSC Ensembl
Innerchr7:21284816..21287051hg19UCSC Ensembl
Innerchr7:21251341..21253576hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382236
hg192236
hg182236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438244, nssv2438246, nssv2438240, nssv2438249, nssv2438245, nssv2438241, nssv2438242, nssv2438247, nssv2438248, nssv2438243
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)nsv981437
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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