A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571842



Internal ID20944913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20435699..20436190hg38UCSC Ensembl
chr6:20435930..20436421hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270154
Samples
Known GenesE2F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571842
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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