A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968649



Internal ID18603877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42663831..42672519hg38UCSC Ensembl
Innerchr9:44340634..44349318hg19UCSC Ensembl
Innerchr9:44280630..44289314hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388689
hg198685
hg188685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2539402, nssv2539397, nssv2539394, nssv2539399, nssv2539403, nssv2539398, nssv2539395, nssv2539401, nssv2539396, nssv2539400
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)nsv968649
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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