A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960086



Internal ID18595339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:30828874..30831432hg38UCSC Ensembl
Innerchr17:29155892..29158450hg19UCSC Ensembl
Innerchr17:26180018..26182576hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382559
hg192559
hg182559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2090218, nssv2090220, nssv2090216, nssv2090213, nssv2090217, nssv2090211, nssv2090212, nssv2090215, nssv2090219, nssv2090214
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)nsv960086
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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