A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572605



Internal ID20945676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155906899..156286533hg38UCSC Ensembl
chr5:155333909..155713543hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38379635
hg19379635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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