A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060085



Internal ID20627125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3903239..3908536hg38UCSC Ensembl
chr1:3819803..3825100hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg385298
hg195298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318128
Supporting Variants
Samples
Known GenesLINC01134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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