A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019346



Internal ID19108564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13176688..13220376hg38UCSC Ensembl
Innerchr8:13034197..13077885hg19UCSC Ensembl
Innerchr8:13078568..13122256hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3843689
hg1943689
hg1843689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7085n100
Supporting Variantsnssv3760199
Samples
Known GenesDLC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019346
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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