A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381840



Internal ID21039393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21334178..21526868hg38UCSC Ensembl
chr5:21334287..21526977hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38192691
hg19192691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128160
Samples
Known GenesGUSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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