A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057066



Internal ID20624106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205829933..205830415hg38UCSC Ensembl
chr1:205799061..205799543hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329500
Supporting Variants
Samples
Known GenesPM20D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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