A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570123



Internal ID20943194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87447634..87447708hg38UCSC Ensembl
chr5:86743451..86743525hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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