A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969590



Internal ID18604817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42906819..42907444hg38UCSC Ensembl
Innerchr9:44063675..44064300hg19UCSC Ensembl
Innerchr9:44003671..44004296hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38626
hg19626
hg18626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2735072, nssv2735073, nssv2735081, nssv2735076, nssv2735077, nssv2735080, nssv2735079, nssv2735078, nssv2735075, nssv2735074
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969590
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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