A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578687



Internal ID20951758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123158165..123158360hg38UCSC Ensembl
chr12:123642712..123642907hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228897
Samples
Known GenesMPHOSPH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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