A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960424



Internal ID18248989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16381541..16382888hg38UCSC Ensembl
Innerchr17:16284855..16286202hg19UCSC Ensembl
Innerchr17:16225580..16226927hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381348
hg191348
hg181348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2079229, nssv2079230, nssv2079234, nssv2079232, nssv2079237, nssv2079228, nssv2079235, nssv2079233, nssv2079236, nssv2079231
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUBB
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960424
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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