A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052699



Internal ID20619739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157534242..157534815hg38UCSC Ensembl
chr1:157504032..157504605hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319720
Supporting Variants
Samples
Known GenesFCRL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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