A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390763



Internal ID21048316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153136879..153159137hg38UCSC Ensembl
chr4:154058031..154080289hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3822259
hg1922259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112047
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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