A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062094



Internal ID20629134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60520595..60521014hg38UCSC Ensembl
chr1:60986267..60986686hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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