A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206885



Internal ID20773925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3549757..3586886hg38UCSC Ensembl
chr2:3597347..3634476hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3837130
hg1937130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336927
Supporting Variants
Samples
Known GenesRNASEH1, RNASEH1-AS1, RPS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206885
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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