A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564848



Internal ID20937919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12646715..21082031hg38UCSC Ensembl
chr9:12646715..21082030hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg388435317
hg198435316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279926
Samples
Known GenesACER2, ADAMTSL1, BNC2, C9orf92, CCDC171, CER1, CNTLN, DENND4C, FAM154A, FLJ41200, FOCAD, FREM1, HAUS6, IFNB1, LINC00583, LOC389705, LURAP1L, MIR3152, MIR4473, MIR4474, MIR491, MLLT3, MPDZ, NFIB, PLIN2, PSIP1, PTPLAD2, RPS6, RRAGA, SCARNA8, SH3GL2, SLC24A2, SNAPC3, TTC39B, TYRP1, ZDHHC21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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