A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726084



Internal ID18677679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59985936..60244806hg38UCSC Ensembl
Innerchr18:57653168..57912039hg19UCSC Ensembl
Innerchr18:55804148..56063019hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38258871
hg19258872
hg18258872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060547
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)nssv3726084
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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