A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203623



Internal ID20770663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33404224..33959487hg38UCSC Ensembl
chr1:33869825..34425088hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38555264
hg19555264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328322
Supporting Variants
Samples
Known GenesCSMD2, HMGB4, LOC402779, ZSCAN20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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