A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390589



Internal ID21048142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157143368..157151240hg38UCSC Ensembl
chr4:158064520..158072392hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387873
hg197873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110979
Samples
Known GenesGLRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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