A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972375



Internal ID18607591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42988838..43075990hg38UCSC Ensembl
Innerchr9:66242575..66329727hg19UCSC Ensembl
Innerchr9:65982395..66069547hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3887153
hg1987153
hg1887153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2546602, nssv2546601, nssv2546599, nssv2546607, nssv2546604, nssv2546600, nssv2546606, nssv2546603, nssv2546605, nssv2546598
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)nsv972375
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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