A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964831



Internal ID18600067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32354324..32355943hg38UCSC Ensembl
Innerchr5:32354430..32356049hg19UCSC Ensembl
Innerchr5:32390187..32391806hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381620
hg191620
hg181620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2351711, nssv2351705, nssv2351712, nssv2351713, nssv2351714, nssv2351710, nssv2351708, nssv2351709, nssv2351707, nssv2351706
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZFR
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964831
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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