A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573623



Internal ID20946694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139230444..139231515hg38UCSC Ensembl
chr4:140151598..140152669hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5475n223
Supporting Variantsnssv18264104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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