A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689559



Internal ID18987840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73232583..73276055hg38UCSC Ensembl
Innerchr8:74144818..74188290hg19UCSC Ensembl
Innerchr8:74307372..74350844hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3843473
hg1943473
hg1843473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019067
Supporting Variants
Samples
Known GenesLOC100130301
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689559
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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