A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948100



Internal ID18594946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80212303..80235396hg38UCSC Ensembl
Innerchr10:81972059..81995152hg19UCSC Ensembl
Innerchr10:81962039..81985132hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
hg1823094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1859683, nssv1859679, nssv1859685, nssv1859682, nssv1859680, nssv1859684, nssv1859678, nssv1859686, nssv1859681, nssv1859687
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00857
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948100
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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