A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972709



Internal ID18607925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65159836..65266917hg38UCSC Ensembl
Innerchr9:42735514..42842285hg19UCSC Ensembl
Innerchr9:42725510..42832281hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38107082
hg19106772
hg18106772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2537127, nssv2537123, nssv2537130, nssv2537121, nssv2537129, nssv2537128, nssv2537126, nssv2537122, nssv2537124, nssv2537125
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)nsv972709
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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