A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972358



Internal ID18607574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61673158..61699748hg38UCSC Ensembl
Innerchr9:44880996..44907586hg19UCSC Ensembl
Innerchr9:44820992..44847582hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3826591
hg1926591
hg1826591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2541744, nssv2541740, nssv2541738, nssv2541741, nssv2541736, nssv2541739, nssv2541742, nssv2541737, nssv2541743, nssv2541735
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)nsv972358
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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