A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052713



Internal ID20619753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157793528..157803460hg38UCSC Ensembl
chr1:157763318..157773250hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389933
hg199933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317147
Supporting Variants
Samples
Known GenesFCRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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