A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065531



Internal ID20632571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86507943..86508592hg38UCSC Ensembl
chr1:86973626..86974275hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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