A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237512



Internal ID20804552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269745..86636480hg38UCSC Ensembl
chr14:77736088..87102824hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389366736
hg199366737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582161
Supporting Variants
Samples
Known GenesADCK1, AHSA1, ALKBH1, C14orf178, CEP128, DIO2, DIO2-AS1, FLRT2, GSTZ1, GTF2A1, ISM2, LINC00911, NGB, NOXRED1, NRXN3, POMT2, SAMD15, SEL1L, SLIRP, SNORA79, SNW1, SPTLC2, STON2, TMED8, TSHR, VIPAS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237512
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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