A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979721



Internal ID20546761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23340342..23374883hg38UCSC Ensembl
chr10:23629271..23663812hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3834542
hg1934542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452011
Supporting Variants
Samples
Known GenesC10orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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