A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569554



Internal ID20942625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29665407..29665801hg38UCSC Ensembl
chr6:29633184..29633578hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6106n223
Supporting Variantsnssv18270528
Samples
Known GenesMOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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