A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963039



Internal ID18598281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34736209..34740507hg38UCSC Ensembl
Innerchr19:35227114..35231412hg19UCSC Ensembl
Innerchr19:39918954..39923252hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384299
hg194299
hg184299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145674, nssv2145669, nssv2145668, nssv2145672, nssv2145667, nssv2145666, nssv2145670, nssv2145675, nssv2145673, nssv2145671
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF181
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963039
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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