A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979894



Internal ID18615095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159386973..159387473hg38UCSC Ensembl
Innerchr3:159104762..159105262hg19UCSC Ensembl
Innerchr3:160587456..160587956hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302339, nssv2302338, nssv2302343, nssv2302341, nssv2302344, nssv2302340, nssv2302336, nssv2302345, nssv2302342, nssv2302337
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979894
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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