A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960413



Internal ID18595664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14176495..14179103hg38UCSC Ensembl
Innerchr17:14079812..14082420hg19UCSC Ensembl
Innerchr17:14020537..14023145hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382609
hg192609
hg182609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2077243, nssv2077774, nssv2077773, nssv2077778, nssv2077775, nssv2077772, nssv2077776, nssv2077242, nssv2077779, nssv2077777
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCOX10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960413
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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