A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025932



Internal ID20592972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52841956..52847478hg38UCSC Ensembl
chr15:53134153..53139675hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385523
hg195523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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