A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587731



Internal ID20960802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62788978..62790372hg38UCSC Ensembl
chr12:63182758..63184152hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225159
Samples
Known GenesPPM1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587731
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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