A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962264



Internal ID18597508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15822831..15880759hg38UCSC Ensembl
Innerchr17:15726145..15784073hg19UCSC Ensembl
Innerchr17:15666870..15724798hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3857929
hg1957929
hg1857929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2079902, nssv2079909, nssv2079905, nssv2079908, nssv2079904, nssv2079910, nssv2079907, nssv2079901, nssv2079903, nssv2079906
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962264
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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