A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960880



Internal ID18596127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57065585..57066184hg38UCSC Ensembl
Innerchr19:57576953..57577552hg19UCSC Ensembl
Innerchr19:62268765..62269364hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38600
hg19600
hg18600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2162012, nssv2162017, nssv2162018, nssv2162019, nssv2162014, nssv2162013, nssv2162011, nssv2162016, nssv2162020, nssv2162015
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960880
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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