A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560917



Internal ID20933988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39956204..39956866hg38UCSC Ensembl
chr8:39813723..39814385hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7320n223
Supporting Variantsnssv18277982
Samples
Known GenesIDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560917
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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