A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561879



Internal ID20934950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155840402..155840787hg38UCSC Ensembl
chr5:155267412..155267797hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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