A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384151



Internal ID21041704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89291067..89299991hg38UCSC Ensembl
chr4:90212218..90221142hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122444
Samples
Known GenesGPRIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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