A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053271



Internal ID20620311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161579455..161661271hg38UCSC Ensembl
chr1:161549245..161631061hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881817
hg1981817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317914
Supporting Variants
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00537


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