A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100919



Internal ID20667959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40022273..40022790hg38UCSC Ensembl
chr3:40063764..40064281hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374247
Supporting Variants
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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