A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560358



Internal ID20933429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56002203..56004095hg38UCSC Ensembl
chr8:56914762..56916654hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381893
hg191893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278291
Samples
Known GenesLYN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560358
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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