A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568282



Internal ID20941353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133017987..133018381hg38UCSC Ensembl
chr5:132353679..132354073hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266674
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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