A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985989



Internal ID20553029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97330671..97331113hg38UCSC Ensembl
chr10:99090428..99090870hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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