A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962297



Internal ID18597541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27272362..27275711hg38UCSC Ensembl
Innerchr17:25599388..25602737hg19UCSC Ensembl
Innerchr17:22623515..22626864hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg383350
hg193350
hg183350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2087353, nssv2087346, nssv2087349, nssv2087354, nssv2087352, nssv2087351, nssv2087355, nssv2087348, nssv2087347, nssv2087350
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)nsv962297
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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