A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059975



Internal ID20627015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28707101..28708300hg38UCSC Ensembl
chr1:29033613..29034812hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323196
Supporting Variants
Samples
Known GenesGMEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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