A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111229



Internal ID15964415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39482960..39511604hg38UCSC Ensembl
Innerchr8:39340479..39369123hg19UCSC Ensembl
Innerchr8:39459636..39488280hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3828645
hg1928645
hg1828645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611066
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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