A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232707



Internal ID20799747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8010736..8011913hg38UCSC Ensembl
chr12:8163332..8164509hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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