A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978808



Internal ID18267325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35356251..35361315hg38UCSC Ensembl
Innerchr19:35847153..35852217hg19UCSC Ensembl
Innerchr19:40538993..40544057hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385065
hg195065
hg185065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2146134, nssv2146133, nssv2146131, nssv2146130, nssv2146128, nssv2146132, nssv2146129, nssv2146127, nssv2146135, nssv2146136
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFFAR3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978808
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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