A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980774



Internal ID20547814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18162930..18164944hg38UCSC Ensembl
chr10:18451859..18453873hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439870
Supporting Variants
Samples
Known GenesCACNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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