A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725276



Internal ID19023557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5012384..5052323hg38UCSC Ensembl
Innerchr18:5012383..5052322hg19UCSC Ensembl
Innerchr18:5002383..5042322hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3839940
hg1939940
hg1839940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059346
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)nssv3725276
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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