A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972751



Internal ID18607967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65254059..65257820hg38UCSC Ensembl
Innerchr9:70147665..70151426hg19UCSC Ensembl
Innerchr9:69437485..69441246hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg383762
hg193762
hg183762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2751880, nssv2749180, nssv2751424, nssv2756280, nssv2755654, nssv2748296, nssv2750126, nssv2746955, nssv2749237, nssv2752201, nssv2746790, nssv2753337, nssv2755819, nssv2753043, nssv2746984, nssv2750785, nssv2749622, nssv2755029, nssv2751143, nssv2753663
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972751
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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