A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234228



Internal ID20801268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94361861..94362200hg38UCSC Ensembl
chr12:94755637..94755976hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582163
Supporting Variants
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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