A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981543



Internal ID18616740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85381073..85382922hg38UCSC Ensembl
Innerchr7:85010389..85012238hg19UCSC Ensembl
Innerchr7:84848325..84850174hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381850
hg191850
hg181850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2467528, nssv2467523, nssv2467526, nssv2467527, nssv2467521, nssv2467520, nssv2467522, nssv2467525, nssv2467519, nssv2467524
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)nsv981543
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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