A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563138



Internal ID20936209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43407311..43407950hg38UCSC Ensembl
chr6:43375049..43375688hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6176n223
Supporting Variantsnssv18271347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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