A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972734



Internal ID18607950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66722800..66744749hg38UCSC Ensembl
Innerchr9:66060206..66082155hg19UCSC Ensembl
Innerchr9:65800026..65821975hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3821950
hg1921950
hg1821950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2546377, nssv2546378, nssv2546373, nssv2546375, nssv2546371, nssv2546379, nssv2546372, nssv2546370, nssv2546376, nssv2546374
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)nsv972734
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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