A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062651



Internal ID20629691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67095358..67095746hg38UCSC Ensembl
chr1:67561041..67561429hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321557
Supporting Variants
Samples
Known GenesC1orf141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00133


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