A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224443



Internal ID20791483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62319349..62320452hg38UCSC Ensembl
chr12:62713130..62714233hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576690
Supporting Variants
Samples
Known GenesUSP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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