A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421506



Internal ID22479376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109333957..109365072hg38UCSC Ensembl
chr6:109655160..109686275hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3831116
hg1931116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421506
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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