A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960835



Internal ID18596082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37779598..37803066hg38UCSC Ensembl
Innerchr19:38270238..38293706hg19UCSC Ensembl
Innerchr19:42962078..42985546hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3823469
hg1923469
hg1823469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2147656, nssv2147660, nssv2147663, nssv2147664, nssv2147661, nssv2147662, nssv2147657, nssv2147655, nssv2147659, nssv2147658
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)nsv960835
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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