A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972721



Internal ID18607937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61822142..61849212hg38UCSC Ensembl
Innerchr9:44958294..44985364hg19UCSC Ensembl
Innerchr9:44898188..44925360hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3827071
hg1927071
hg1827173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2541832, nssv2541833, nssv2541840, nssv2541838, nssv2541836, nssv2541839, nssv2541837, nssv2541835, nssv2541834, nssv2541841
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)nsv972721
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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