A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980382



Internal ID20547422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44960893..44966266hg38UCSC Ensembl
chr10:45456341..45461714hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385374
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455481
Supporting Variants
Samples
Known GenesRASSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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