A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111094



Internal ID15964280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39563676hg38UCSC Ensembl
Innerchr8:39237668..39421195hg19UCSC Ensembl
Innerchr8:39356825..39540352hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38183528
hg19183528
hg18183528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611015
Supporting Variants
Samples
Known GenesADAM3A, ADAM5, LOC100130964
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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