A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2210n223



Internal ID22805178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77012562..78083055hg38UCSC Ensembl
chr14:77478905..78549398hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381070494
hg191070494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577345, nsv6577827, nsv6593620
Samples
Known GenesADCK1, AHSA1, ALKBH1, C14orf178, GSTZ1, IRF2BPL, ISM2, KIAA1737, MIR1260A, NGB, NOXRED1, POMT2, SAMD15, SLIRP, SNW1, SPTLC2, TMED8, TMEM63C, VIPAS39, ZDHHC22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2210n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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