A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2598n223



Internal ID22805566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77980072..78773099hg38UCSC Ensembl
chr15:78272414..79065441hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38793028
hg19793028
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6589383, nsv6579298, nsv6592260, nsv6587762
Samples
Known GenesACSBG1, ADAMTS7, CHRNA3, CHRNA5, CHRNB4, CIB2, CRABP1, DNAJA4, HYKK, IDH3A, IREB2, LOC646938, LOC91450, MIR5003, PSMA4, SH2D7, TBC1D2B, WDR61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2598n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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