A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969587



Internal ID18604814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42949654..42950654hg38UCSC Ensembl
Innerchr9:44020465..44021465hg19UCSC Ensembl
Innerchr9:43960461..43961461hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2734062, nssv2734070, nssv2734068, nssv2734071, nssv2734066, nssv2734063, nssv2734065, nssv2734069, nssv2734064, nssv2734067
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969587
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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