A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972637



Internal ID18607853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93226..121450hg38UCSC Ensembl
Innerchr9:93226..121450hg19UCSC Ensembl
Innerchr9:83226..111450hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3828225
hg1928225
hg1828225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2519325, nssv2519321, nssv2519318, nssv2519327, nssv2519320, nssv2519324, nssv2519319, nssv2519323, nssv2519322, nssv2519326
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD1, FOXD4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972637
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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