A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725290



Internal ID19023571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9995048..10115536hg38UCSC Ensembl
Innerchr18:9995045..10115533hg19UCSC Ensembl
Innerchr18:9985045..10105533hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38120489
hg19120489
hg18120489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058492
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)nssv3725290
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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