A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565171



Internal ID20938242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124489634..124490511hg38UCSC Ensembl
chr8:125501875..125502752hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276154
Samples
Known GenesTATDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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