A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968665



Internal ID18257207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62249739..62386182hg38UCSC Ensembl
Innerchr9:46561040..46697483hg19UCSC Ensembl
Innerchr9:46400757..46537479hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38136444
hg19136444
hg18136723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2544173, nssv2544179, nssv2544176, nssv2544174, nssv2544182, nssv2544180, nssv2544175, nssv2544178, nssv2544181, nssv2544177
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968665
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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