A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757254



Internal ID19055535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50148335..50186248hg38UCSC Ensembl
Innerchr8:51060895..51098808hg19UCSC Ensembl
Innerchr8:51223448..51261361hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3837914
hg1937914
hg1837914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027984
Supporting Variants
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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