A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027865



Internal ID18770396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91106767..91167737hg38UCSC Ensembl
Innerchr8:92118995..92179965hg19UCSC Ensembl
Innerchr8:92188171..92249141hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3860971
hg1960971
hg1860971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7268n100
Supporting Variantsnssv3689713
Samples
Known GenesLRRC69
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027865
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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