A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973369



Internal ID18608584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65277761..65282353hg38UCSC Ensembl
Innerchr9:70171367..70175959hg19UCSC Ensembl
Innerchr9:69461187..69465779hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384593
hg194593
hg184593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2747508, nssv2748399, nssv2752632, nssv2756629, nssv2750135, nssv2748303, nssv2755033, nssv2751830, nssv2755237, nssv2750596
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXD4L5
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973369
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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