A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090131



Internal ID20657171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67218248..67224470hg38UCSC Ensembl
chr2:67445380..67451602hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg386223
hg196223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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