A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433602



Internal ID22491472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41028668..41028719hg38UCSC Ensembl
chr6:40996407..40996458hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900505
Supporting Variants
Samples
Known GenesUNC5CL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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