A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090493



Internal ID20657533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98874983..98877984hg38UCSC Ensembl
chr2:99491446..99494447hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337700
Supporting Variants
Samples
Known GenesKIAA1211L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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