A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082002



Internal ID20649042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17560794..17561471hg38UCSC Ensembl
chr2:17742061..17742738hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354008
Supporting Variants
Samples
Known GenesVSNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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