A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689023



Internal ID18987304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39389580..39475602hg38UCSC Ensembl
Innerchr8:39247099..39333121hg19UCSC Ensembl
Innerchr8:39366256..39452278hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3886023
hg1986023
hg1886023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021847
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689023
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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