A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568299



Internal ID20941370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124425508..124546681hg38UCSC Ensembl
chr5:123761201..123882374hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38121174
hg19121174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5930n223
Supporting Variantsnssv18266239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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