A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982401



Internal ID20549441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65917018..65917416hg38UCSC Ensembl
chr10:67676776..67677174hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00103


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