A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233960



Internal ID20801001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43440187..43440824hg38UCSC Ensembl
chr12:43833990..43834627hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591938
Supporting Variants
Samples
Known GenesADAMTS20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer