A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564567



Internal ID20937638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95608286..95608648hg38UCSC Ensembl
chr5:94943990..94944352hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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