A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977397



Internal ID20544438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108367901..108376300hg38UCSC Ensembl
chr10:110127659..110136058hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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