A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960768



Internal ID18596015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:190564..204264hg38UCSC Ensembl
Innerchr19:190564..204264hg19UCSC Ensembl
Innerchr19:141564..155264hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813701
hg1913701
hg1813701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2663693, nssv2663694, nssv2663382, nssv2663383, nssv2663696, nssv2663384, nssv2663697, nssv2663698, nssv2663695, nssv2663699
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC01002
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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