A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051511



Internal ID20618551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13501502..13501687hg38UCSC Ensembl
chr1:13827952..13828141hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38186
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329940
Supporting Variants
Samples
Known GenesLRRC38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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