A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725319



Internal ID19023600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39808481..39846180hg38UCSC Ensembl
Innerchr18:37388445..37426144hg19UCSC Ensembl
Innerchr18:35642443..35680142hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3837700
hg1937700
hg1837700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065211
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)nssv3725319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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