A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982899



Internal ID18271408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76488132..76498717hg38UCSC Ensembl
Innerchr10:78247890..78258475hg19UCSC Ensembl
Innerchr10:77917896..77928481hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3810586
hg1910586
hg1810586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765236, nssv2758628, nssv2763883, nssv2765845, nssv2762219, nssv2763748
SamplesHGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00456
Known GenesC10orf11
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982899
Frequency
Sample Size10
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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