A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960146



Internal ID18248713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68187319..68207176hg38UCSC Ensembl
Innerchr17:66183460..66203317hg19UCSC Ensembl
Innerchr17:63695055..63714912hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3819858
hg1919858
hg1819858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2110770, nssv2110773, nssv2110764, nssv2110765, nssv2110771, nssv2110769, nssv2110767, nssv2110768, nssv2110772, nssv2110766
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC440461
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960146
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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