A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977158



Internal ID20544198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100237191..100237580hg38UCSC Ensembl
chr10:101996948..101997337hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442660
Supporting Variants
Samples
Known GenesCWF19L1, SNORA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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