A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403239



Internal ID21060792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151891641..151990892hg38UCSC Ensembl
chr5:151271202..151370453hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3899252
hg1999252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213303
Samples
Known GenesGLRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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