A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972462



Internal ID18607678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134102159..134127157hg38UCSC Ensembl
Innerchr9:136967281..136992279hg19UCSC Ensembl
Innerchr9:135957102..135982100hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3824999
hg1924999
hg1824999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2569703, nssv2569699, nssv2569698, nssv2569701, nssv2569696, nssv2569694, nssv2569697, nssv2569700, nssv2569695, nssv2569702
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)nsv972462
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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