A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441520



Internal ID22499390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55153737..55165793hg38UCSC Ensembl
chr6:55018535..55030591hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3812057
hg1912057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441520
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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