A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972665



Internal ID18607881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34998167..34999237hg38UCSC Ensembl
Innerchr9:34998164..34999234hg19UCSC Ensembl
Innerchr9:34988164..34989234hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381071
hg191071
hg181071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527532, nssv2527531, nssv2527528, nssv2527530, nssv2527526, nssv2527535, nssv2527527, nssv2527533, nssv2527529, nssv2527534
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDNAJB5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972665
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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