A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981862



Internal ID20548902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:501218..552199hg38UCSC Ensembl
chr10:547158..598139hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3850982
hg1950982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440751
Supporting Variants
Samples
Known GenesDIP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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