A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962265



Internal ID18250823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16161098..16171399hg38UCSC Ensembl
Innerchr17:16064412..16074713hg19UCSC Ensembl
Innerchr17:16005137..16015438hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3810302
hg1910302
hg1810302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2080074, nssv2080077, nssv2080069, nssv2080068, nssv2080075, nssv2080072, nssv2080070, nssv2080071, nssv2080073, nssv2080076
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNCOR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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