A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689529



Internal ID18987810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72383595..72471092hg38UCSC Ensembl
Innerchr8:73295830..73383327hg19UCSC Ensembl
Innerchr8:73458384..73545881hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3887498
hg1987498
hg1887498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022079
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)nssv3689529
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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