A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980793



Internal ID20547833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18455428..18463013hg38UCSC Ensembl
chr10:18744357..18751942hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg387586
hg197586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437732
Supporting Variants
Samples
Known GenesCACNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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