A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964986



Internal ID18600221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178723595..178724567hg38UCSC Ensembl
Innerchr5:178150596..178151568hg19UCSC Ensembl
Innerchr5:178083202..178084174hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38973
hg19973
hg18973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2388981, nssv2388973, nssv2388975, nssv2388977, nssv2388972, nssv2388979, nssv2388978, nssv2388976, nssv2388974, nssv2388980
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF354A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964986
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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