A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205433



Internal ID20772473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191150347..191162072hg38UCSC Ensembl
chr2:192015073..192026798hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3811726
hg1911726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339570
Supporting Variants
Samples
Known GenesSTAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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