A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575582



Internal ID20948653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14768432..14768917hg38UCSC Ensembl
chr6:14768663..14769148hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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