A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111258



Internal ID15964444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40012322..40023247hg38UCSC Ensembl
Innerchr8:39869841..39880766hg19UCSC Ensembl
Innerchr8:39988998..39999923hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810926
hg1910926
hg1810926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611088
Supporting Variants
Samples
Known GenesIDO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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