A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558274



Internal ID20931345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1741536..1742068hg38UCSC Ensembl
chr6:1741770..1742302hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269998
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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