A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567988



Internal ID20941059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56988228..56988875hg38UCSC Ensembl
chr6:56853026..56853673hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270981
Samples
Known GenesBEND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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