A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984135



Internal ID20551175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82232333..82339613hg38UCSC Ensembl
chr10:83992089..84099369hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38107281
hg19107281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453122
Supporting Variants
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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