A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587762



Internal ID20960833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77980072..78773098hg38UCSC Ensembl
chr15:78272414..79065440hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38793027
hg19793027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2598n223
Supporting Variantsnssv18239712
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)nsv6587762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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