A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061625



Internal ID20628665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47882507..47901032hg38UCSC Ensembl
chr1:48348179..48366704hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3818526
hg1918526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315638
Supporting Variants
Samples
Known GenesTRABD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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