A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556077



Internal ID20929148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144890683..144891644hg38UCSC Ensembl
chr6:145211819..145212780hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6444n223
Supporting Variantsnssv18273183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556077
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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