A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563752



Internal ID20936823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53149483..53150486hg38UCSC Ensembl
chr6:53014281..53015284hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6186n223
Supporting Variantsnssv18271508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563752
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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