A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963094



Internal ID18598336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58592790..58599416hg38UCSC Ensembl
Innerchr19:59104157..59110783hg19UCSC Ensembl
Innerchr19:63795969..63802595hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386627
hg196627
hg186627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2661680, nssv2661682, nssv2661677, nssv2661674, nssv2661676, nssv2661681, nssv2661679, nssv2661673, nssv2661678, nssv2661675
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963094
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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