A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420489



Internal ID22478359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12393047..12393955hg38UCSC Ensembl
chr6:12393279..12394187hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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