A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685336



Internal ID18983617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21406467..21445678hg38UCSC Ensembl
Innerchr8:21263978..21303189hg19UCSC Ensembl
Innerchr8:21308258..21347469hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3839212
hg1939212
hg1839212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019288
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)nssv3685336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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