A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968671



Internal ID18603899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62710392..62712526hg38UCSC Ensembl
Innerchr9:47021693..47023827hg19UCSC Ensembl
Innerchr9:46861513..46863647hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg382135
hg192135
hg182135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2545478, nssv2545479, nssv2545477, nssv2545483, nssv2545482, nssv2545484, nssv2545485, nssv2545480, nssv2545481, nssv2545486
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)nsv968671
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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