A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555882



Internal ID329031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45580124..46272839hg38UCSC Ensembl
chr19:46083382..46776096hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38692716
hg19692715
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723589
Samples
Known GenesC19orf83, CCDC61, DKFZp434J0226, DMPK, DMWD, EML2, FBXO46, FOXA3, GIPR, GPR4, IGFL1, IGFL2, IGFL3, IGFL4, IRF2BP1, LOC388553, MIR330, MIR642A, MIR642B, MIR769, MYPOP, NANOS2, NOVA2, OPA3, PGLYRP1, QPCTL, RNU6-66P, RSPH6A, SIX5, SNRPD2, SYMPK
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555882
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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