A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560975



Internal ID20934046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20164..205286hg38UCSC Ensembl
chr5:20164..205401hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38185123
hg19185238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266296
Samples
Known GenesCCDC127, LRRC14B, PLEKHG4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560975
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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