A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739639



Internal ID19037920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18155335..18211140hg38UCSC Ensembl
Innerchr3:18196827..18252632hg19UCSC Ensembl
Innerchr3:18171831..18227636hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3855806
hg1955806
hg1855806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011305
Supporting Variants
Samples
Known GenesLOC339862
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739639
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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