A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573747



Internal ID20946818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16790206..16802637hg38UCSC Ensembl
chr4:16791829..16804260hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3812432
hg1912432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264346
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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