A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060125



Internal ID20627165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39880735..39888431hg38UCSC Ensembl
chr1:40346407..40354103hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg387697
hg197697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330017
Supporting Variants
Samples
Known GenesTRIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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