A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178037



Internal ID20745077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30145801..30191700hg38UCSC Ensembl
chr18:27725766..27771665hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3845900
hg1945900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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