A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573322



Internal ID20946393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139497347..139497860hg38UCSC Ensembl
chr4:140418501..140419014hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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