A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760199



Internal ID19058480
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 StatusS
Merged Variantsnsv1019346
Supporting Variants
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)nssv3760199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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