A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981925



Internal ID20548965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55013054..55325703hg38UCSC Ensembl
chr10:56772814..57085463hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38312650
hg19312650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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