A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233210



Internal ID20800250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101812609..101813105hg38UCSC Ensembl
chr12:102206387..102206883hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584859
Supporting Variants
Samples
Known GenesGNPTAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233210
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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