A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432485



Internal ID22490355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33912123..33912174hg38UCSC Ensembl
chr6:33879900..33879951hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432485
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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