A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978757



Internal ID18613960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:113626..153376hg38UCSC Ensembl
Innerchr19:113626..153376hg19UCSC Ensembl
Innerchr19:64626..104376hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839751
hg1939751
hg1839751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2128143, nssv2128147, nssv2128148, nssv2128152, nssv2128145, nssv2128150, nssv2128146, nssv2128151, nssv2128149, nssv2128144
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)nsv978757
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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