A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972398



Internal ID18607614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71589086..71590305hg38UCSC Ensembl
Innerchr9:74204002..74205221hg19UCSC Ensembl
Innerchr9:73393822..73395041hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381220
hg191220
hg181220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552693, nssv2552689, nssv2552692, nssv2552695, nssv2552687, nssv2552690, nssv2552691, nssv2552694, nssv2552688, nssv2552686
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972398
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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