A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979639



Internal ID20546679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21888813..21894107hg38UCSC Ensembl
chr10:22177742..22183036hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385295
hg195295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454707
Supporting Variants
Samples
Known GenesDNAJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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