A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980332



Internal ID20547372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44331921..44345183hg38UCSC Ensembl
chr10:44827369..44840631hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813263
hg1913263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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