A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753995



Internal ID16047951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92935860..93050908hg38UCSC Ensembl
Innerchr10:94695617..94810665hg19UCSC Ensembl
Innerchr10:94685597..94800655hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38115049
hg19115049
hg18115059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551942
Supporting Variants
Samples
Known GenesEXOC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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