A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964988



Internal ID18600223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178922099..178926457hg38UCSC Ensembl
Innerchr5:178349100..178353458hg19UCSC Ensembl
Innerchr5:178281706..178286064hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384359
hg194359
hg184359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2389966, nssv2389959, nssv2389967, nssv2389964, nssv2389963, nssv2389965, nssv2389962, nssv2389960, nssv2389958, nssv2389961
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZFP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964988
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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