A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960071



Internal ID18595324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19024288..19025116hg38UCSC Ensembl
Innerchr17:18927601..18928429hg19UCSC Ensembl
Innerchr17:18868326..18869154hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38829
hg19829
hg18829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2083664, nssv2083667, nssv2083663, nssv2083666, nssv2083659, nssv2083668, nssv2083661, nssv2083665, nssv2083660, nssv2083662
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGRAP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960071
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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