A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963364



Internal ID18251919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141925659..141926159hg38UCSC Ensembl
Innerchr3:141644501..141645001hg19UCSC Ensembl
Innerchr3:143127191..143127691hg18UCSC Ensembl
Cytoband3q23
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 Variantsnssv2298081, nssv2298080, nssv2298086, nssv2298083, nssv2298077, nssv2298079, nssv2298084, nssv2298078, nssv2298085, nssv2298082
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesATP1B3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963364
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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