A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979741



Internal ID20546781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23593873..23597065hg38UCSC Ensembl
chr10:23882802..23885994hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383193
hg193193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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