A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210372



Internal ID20777412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158094001..158119800hg38UCSC Ensembl
chr3:157811790..157837589hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3825800
hg1925800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366053
Supporting Variants
Samples
Known GenesRSRC1, SHOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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