A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900555



Internal ID1159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33534637..33534637hg38UCSC Ensembl
chr1:34000237..34000237hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543134
Supporting Variants
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900555
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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