A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124912



Internal ID15978098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142241748..142323928hg38UCSC Ensembl
Innerchr8:143323109..143405289hg19UCSC Ensembl
Innerchr8:143321016..143403196hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3882181
hg1982181
hg1882181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612692
Supporting Variants
Samples
Known GenesTSNARE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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