A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562794



Internal ID20935865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81742178..81743115hg38UCSC Ensembl
chr6:82451895..82452832hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6294n223
Supporting Variantsnssv18274739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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