A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685567



Internal ID18983848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36449913..36581647hg38UCSC Ensembl
Innerchr8:36307431..36439165hg19UCSC Ensembl
Innerchr8:36426589..36558323hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38131735
hg19131735
hg18131735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015637
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)nssv3685567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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