A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723224



Internal ID19021505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73359697..73493610hg38UCSC Ensembl
Innerchr18:71026932..71160845hg19UCSC Ensembl
Innerchr18:69177912..69311825hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38133914
hg19133914
hg18133914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064152
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)nssv3723224
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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