A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962262



Internal ID18597506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15698007..15706307hg38UCSC Ensembl
Innerchr17:15601321..15609621hg19UCSC Ensembl
Innerchr17:15542046..15550346hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg388301
hg198301
hg188301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2080949, nssv2080951, nssv2080953, nssv2080956, nssv2080954, nssv2080955, nssv2080952, nssv2080950, nssv2080957, nssv2080948
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF286A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962262
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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