A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206899



Internal ID20773939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37051305..37094890hg38UCSC Ensembl
chr2:37278448..37322033hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3843586
hg1943586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350616
Supporting Variants
Samples
Known GenesGPATCH11, HEATR5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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