A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592755



Internal ID20965826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15512232..15512710hg38UCSC Ensembl
chr12:15665166..15665644hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237114
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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