A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960864



Internal ID18249425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53115707..53116460hg38UCSC Ensembl
Innerchr19:53618960..53619713hg19UCSC Ensembl
Innerchr19:58310772..58311525hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38754
hg19754
hg18754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2157491, nssv2157485, nssv2157484, nssv2157489, nssv2157490, nssv2157482, nssv2157486, nssv2157483, nssv2157487, nssv2157488
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF415
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960864
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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