A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223704



Internal ID20790744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50509662..51212481hg38UCSC Ensembl
chr14:50976380..51679199hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38702820
hg19702820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587501
Supporting Variants
Samples
Known GenesABHD12B, ATL1, MAP4K5, NIN, PYGL, SAV1, TRIM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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