A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357364



Internal ID22583033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225420036..225421221hg38UCSC Ensembl
chr1:225607738..225608923hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381186
hg191186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885277
Supporting Variants
Samples
Known GenesLBR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357364
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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