A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081709



Internal ID20648749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18372790..18381512hg38UCSC Ensembl
chr2:18554056..18562778hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg388723
hg198723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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