A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543056



Internal ID20916307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101673856..101674069hg38UCSC Ensembl
chr3:101392700..101392913hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259485
Samples
Known GenesZBTB11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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