A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229091



Internal ID20796131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29345899..29346063hg38UCSC Ensembl
chr12:29498832..29498996hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582784
Supporting Variants
Samples
Known GenesERGIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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