A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968634



Internal ID18603862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39811196..39831080hg38UCSC Ensembl
Innerchr9:41956214..41976098hg19UCSC Ensembl
Innerchr9:41946214..41966098hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3819885
hg1919885
hg1819885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2535032, nssv2535026, nssv2535030, nssv2535034, nssv2535025, nssv2535027, nssv2535029, nssv2535028, nssv2535031, nssv2535033
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968634
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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