A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599210



Internal ID20972281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37175514..37175882hg38UCSC Ensembl
chr21:38547816..38548184hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254719
Samples
Known GenesTTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599210
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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