A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187079



Internal ID20754119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82658683..82736457hg38UCSC Ensembl
chr10:84418439..84496213hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3877775
hg1977775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445223
Supporting Variants
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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