A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111156



Internal ID15964342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39403008..39492792hg38UCSC Ensembl
Innerchr8:39260527..39350311hg19UCSC Ensembl
Innerchr8:39379684..39469468hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3889785
hg1989785
hg1889785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611036
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)nssv1111156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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