A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559115



Internal ID20932186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153356513..153356566hg38UCSC Ensembl
chr4:154277665..154277718hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263888
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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