A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960832



Internal ID18249393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37028939..37062279hg38UCSC Ensembl
Innerchr19:37519841..37553181hg19UCSC Ensembl
Innerchr19:42211681..42245021hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3833341
hg1933341
hg1833341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2147237, nssv2147230, nssv2147229, nssv2147228, nssv2147231, nssv2147234, nssv2147233, nssv2147232, nssv2147236, nssv2147235
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)nsv960832
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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