A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562613



Internal ID20935684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123146760..123147907hg38UCSC Ensembl
chr8:124159000..124160147hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7483n223
Supporting Variantsnssv18275522
Samples
Known GenesTBC1D31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562613
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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