A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556047



Internal ID20929118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124492315..124492689hg38UCSC Ensembl
chr8:125504556..125504930hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276157
Samples
Known GenesTATDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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