A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981445



Internal ID20548485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4069069..4070358hg38UCSC Ensembl
chr10:4111261..4112550hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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