A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962307



Internal ID18250865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31221313..31233000hg38UCSC Ensembl
Innerchr17:29548331..29560018hg19UCSC Ensembl
Innerchr17:26572457..26584144hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3811688
hg1911688
hg1811688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2090513, nssv2090514, nssv2090515, nssv2090509, nssv2090512, nssv2090517, nssv2090510, nssv2090511, nssv2090508, nssv2090516
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962307
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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