A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751742



Internal ID15699012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78264137..78295813hg38UCSC Ensembl
Innerchr10:80023894..80055570hg19UCSC Ensembl
Innerchr10:79693900..79725576hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3831677
hg1931677
hg1831677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551560
Supporting Variants
Samples
Known GenesLINC00595
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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