A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567636



Internal ID20940707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54555777..54810711hg38UCSC Ensembl
chr4:55421944..55676877hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38254935
hg19254934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266416
Samples
Known GenesKIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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