A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088775



Internal ID20655815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5966112..5969609hg38UCSC Ensembl
chr2:6106244..6109741hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg383498
hg193498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350842
Supporting Variants
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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