A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569931



Internal ID20943002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78606848..78608741hg38UCSC Ensembl
chr5:77902671..77904564hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381894
hg191894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270274
Samples
Known GenesLHFPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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