A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556713



Internal ID20929784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128148442..128148905hg38UCSC Ensembl
chr4:129069597..129070060hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263000
Samples
Known GenesLARP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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