A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060343



Internal ID20627383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30802588..30808747hg38UCSC Ensembl
chr1:31275435..31281594hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg386160
hg196160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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