A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963023



Internal ID18598265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21309190..21387593hg38UCSC Ensembl
Innerchr19:21491992..21570395hg19UCSC Ensembl
Innerchr19:21283832..21362235hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3878404
hg1978404
hg1878404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2140385, nssv2140386, nssv2140388, nssv2140389, nssv2140382, nssv2140384, nssv2140390, nssv2140383, nssv2140387, nssv2140391
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF708, ZNF738
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963023
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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