A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968670



Internal ID18603898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62690251..62709729hg38UCSC Ensembl
Innerchr9:47001552..47021030hg19UCSC Ensembl
Innerchr9:46841372..46860850hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3819479
hg1919479
hg1819479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2544613, nssv2544610, nssv2544612, nssv2544611, nssv2544605, nssv2544608, nssv2544606, nssv2544609, nssv2544607, nssv2544614
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)nsv968670
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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