A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980834



Internal ID20547874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4648712..4650505hg38UCSC Ensembl
chr10:4690904..4692697hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436520
Supporting Variants
Samples
Known GenesLINC00704
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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