A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212737



Internal ID20779777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15701618..15710131hg38UCSC Ensembl
chr4:15703241..15711754hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg388514
hg198514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372595
Supporting Variants
Samples
Known GenesBST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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