A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561164



Internal ID20934235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42507958..42508599hg38UCSC Ensembl
chr8:42365476..42366117hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278045
Samples
Known GenesSLC20A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561164
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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