A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033160



Internal ID19122382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85098408..85118325hg38UCSC Ensembl
Innerchr8:86010643..86030560hg19UCSC Ensembl
Innerchr8:86197895..86217812hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3819918
hg1919918
hg1819918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757308
Samples
Known GenesLRRCC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033160
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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