A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027617



Internal ID19116836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142328189..142373088hg38UCSC Ensembl
Innerchr8:143409550..143454449hg19UCSC Ensembl
Innerchr8:143407457..143452356hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3844900
hg1944900
hg1844900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690089
Samples
Known GenesTSNARE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027617
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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