A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962392



Internal ID18597636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26935981..26941323hg38UCSC Ensembl
Innerchr17:25263007..25268349hg19UCSC Ensembl
Innerchr17:22286857..22292476hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg385343
hg195343
hg185620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2655128, nssv2655121, nssv2655129, nssv2655779, nssv2655772, nssv2655124, nssv2655126, nssv2655771, nssv2655770, nssv2655123, nssv2655127, nssv2655776, nssv2655125, nssv2655120, nssv2655122, nssv2655778, nssv2655773, nssv2655774, nssv2655775, nssv2655777
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)nsv962392
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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