A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085198



Internal ID20652238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30589907..30627392hg38UCSC Ensembl
chr2:30812773..30850258hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3837486
hg1937486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339663
Supporting Variants
Samples
Known GenesLCLAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00059


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