A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237672



Internal ID20804712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91074052..93300799hg38UCSC Ensembl
chr14:91540396..93767145hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg382226748
hg192226750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591551
Supporting Variants
Samples
Known GenesATXN3, BTBD7, C14orf142, C14orf159, CATSPERB, CCDC88C, CHGA, CPSF2, FBLN5, GOLGA5, GPR68, ITPK1, ITPK1-AS1, LGMN, MOAP1, NDUFB1, RIN3, SLC24A4, SMEK1, SNORA11B, TC2N, TMEM251, TRIP11, UBR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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