A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571563



Internal ID20944634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3679800..4779377hg38UCSC Ensembl
chr5:3679914..4779490hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381099578
hg191099577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268838
Samples
Known GenesLOC101929153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571563
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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