A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685507



Internal ID18983788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25654546..25726813hg38UCSC Ensembl
Innerchr8:25512062..25584329hg19UCSC Ensembl
Innerchr8:25567979..25640246hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3872268
hg1972268
hg1872268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031625
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)nssv3685507
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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