A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071696



Internal ID21460928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82106153..82106217hg38UCSC Ensembl
chr10:83865909..83865973hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586416
Supporting Variants
SamplesHG02818
Known GenesNRG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071696
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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