A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419193



Internal ID22477063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138104867..138104957hg38UCSC Ensembl
chr6:138426004..138426094hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905993
Supporting Variants
Samples
Known GenesPERP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419193
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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