A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237186



Internal ID20804226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61789117..61790761hg38UCSC Ensembl
chr14:62255835..62257479hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576063
Supporting Variants
Samples
Known GenesSNAPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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