A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083418



Internal ID20650458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214493873..214494978hg38UCSC Ensembl
chr2:215358597..215359702hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346851
Supporting Variants
Samples
Known GenesVWC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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