A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579598



Internal ID20952669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75227706..75760489hg38UCSC Ensembl
chr15:75520047..76052830hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38532784
hg19532784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2583n223
Supporting Variantsnssv18241960
Samples
Known GenesCOMMD4, CSPG4, DNM1P35, GOLGA6C, GOLGA6D, IMP3, MAN2C1, MIR631, NEIL1, ODF3L1, PTPN9, SIN3A, SNUPN, SNX33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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