A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691456



Internal ID18989737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115042063..115141777hg38UCSC Ensembl
Innerchr8:116054292..116154006hg19UCSC Ensembl
Innerchr8:116123468..116223182hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3899715
hg1999715
hg1899715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016140
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)nssv3691456
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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