A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982352



Internal ID18617547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133338914..133339514hg38UCSC Ensembl
Innerchr9:136205751..136206351hg19UCSC Ensembl
Innerchr9:135195572..135196172hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38601
hg19601
hg18601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2569522, nssv2569523, nssv2569529, nssv2569531, nssv2569528, nssv2569524, nssv2569525, nssv2569526, nssv2569530, nssv2569527
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)nsv982352
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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