A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968595



Internal ID18603823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8712523..8714059hg38UCSC Ensembl
Innerchr9:8712523..8714059hg19UCSC Ensembl
Innerchr9:8702523..8704059hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381537
hg191537
hg181537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522657, nssv2522654, nssv2522659, nssv2522652, nssv2522653, nssv2522655, nssv2522656, nssv2522658, nssv2522651, nssv2522650
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPTPRD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968595
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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