A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050797



Internal ID20617837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106816208..106819666hg38UCSC Ensembl
chr1:107358830..107362288hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383459
hg193459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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