A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2762219



Internal ID17482454
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 Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982899
Supporting Variants
SamplesHGDP00998
Known GenesC10orf11
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2762219
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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