A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564632



Internal ID20937703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17108832..17109410hg38UCSC Ensembl
chr5:17108941..17109519hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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