A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568127



Internal ID20941198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164228197..164228330hg38UCSC Ensembl
chr5:163655203..163655336hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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