A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366006



Internal ID22591675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193038753..193038887hg38UCSC Ensembl
chr1:193007883..193008017hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872650
Supporting Variants
Samples
Known GenesUCHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366006
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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