A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559866



Internal ID332886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62865770..63725218hg38UCSC Ensembl
chr20:61497122..62356570hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38859449
hg19859449
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733610
Samples
Known GenesARFGAP1, ARFRP1, BHLHE23, BIRC7, C20orf195, CHRNA4, COL20A1, DIDO1, EEF1A2, FLJ16779, GID8, GMEB2, HAR1A, HAR1B, HELZ2, KCNQ2, LINC00029, LINC01056, LOC63930, MIR124-3, MIR3196, MIR4326, NKAIN4, PPDPF, PTK6, RTEL1, RTEL1-TNFRSF6B, SLC17A9, SRMS, STMN3, TNFRSF6B, YTHDF1, ZGPAT
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559866
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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