A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602115



Internal ID21794162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35414234..38834329hg38UCSC Ensembl
chr14:35883440..39303533hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383420096
hg193420094
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106211
Supporting Variants
Samples
Known GenesBRMS1L, CLEC14A, FOXA1, INSM2, LINC00609, LINC00639, MBIP, MIPOL1, MIR4503, NKX2-1, NKX2-1-AS1, NKX2-8, PAX9, PTCSC3, RALGAPA1, RALGAPA1P, SFTA3, SLC25A21, SLC25A21-AS1, SSTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602115
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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