A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117950



Internal ID15971136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96506697..96509103hg38UCSC Ensembl
Innerchr8:97518925..97521331hg19UCSC Ensembl
Innerchr8:97588101..97590507hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382407
hg192407
hg182407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611775
Supporting Variants
Samples
Known GenesSDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1117950
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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