A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977237



Internal ID20544277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102094141..102098004hg38UCSC Ensembl
chr10:103853898..103857761hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383864
hg193864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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