A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217195



Internal ID20784235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19258850..19259446hg38UCSC Ensembl
chr12:19411784..19412380hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583852
Supporting Variants
Samples
Known GenesPLEKHA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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