A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579298



Internal ID20952369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77987246..78765455hg38UCSC Ensembl
chr15:78279588..79057797hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38778210
hg19778210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2598n223
Supporting Variantsnssv18239714
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)nsv6579298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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