A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972748



Internal ID18607964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65166952..65251516hg38UCSC Ensembl
Innerchr9:70060552..70145122hg19UCSC Ensembl
Innerchr9:69350372..69434942hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3884565
hg1984571
hg1884571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2549665, nssv2549660, nssv2549668, nssv2549663, nssv2549666, nssv2549669, nssv2549667, nssv2549664, nssv2549662, nssv2549661
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)nsv972748
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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