A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567060



Internal ID20940131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122595849..122596418hg38UCSC Ensembl
chr4:123517004..123517573hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567060
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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