A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562416



Internal ID20935487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133836995..133838381hg38UCSC Ensembl
chr6:134158133..134159519hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381387
hg191387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6407n223
Supporting Variantsnssv18271911
Samples
Known GenesMGC34034
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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