A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571852



Internal ID20944923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147215473..147216314hg38UCSC Ensembl
chr6:147536609..147537450hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273217
Samples
Known GenesSTXBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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