A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557415



Internal ID20930486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233406..40235438hg38UCSC Ensembl
chr4:40235026..40237058hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265243
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557415
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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