A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689469



Internal ID18987750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61126514..61188564hg38UCSC Ensembl
Innerchr8:62039073..62101123hg19UCSC Ensembl
Innerchr8:62201627..62263677hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3862051
hg1962051
hg1862051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026243
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689469
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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