A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177256



Internal ID20744296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40468774..40604074hg38UCSC Ensembl
chr18:38048738..38184038hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38135301
hg19135301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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