A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234407



Internal ID20801447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70658905..70659999hg38UCSC Ensembl
chr12:71052685..71053779hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587710
Supporting Variants
Samples
Known GenesPTPRR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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