A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556729



Internal ID20929800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56219023..56219489hg38UCSC Ensembl
chr8:57131582..57132048hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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