A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556848



Internal ID20929919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90743255..92932434hg38UCSC Ensembl
chr9:93505537..95694716hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382189180
hg192189180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281393
Samples
Known GenesANKRD19P, ASPN, AUH, BICD2, CENPP, ECM2, IARS, IPPK, LINC00475, LOC100128076, LOC100128361, LOC100129316, MIR3651, MIR3910-1, MIR3910-2, MIR4670, NFIL3, NOL8, OGN, OMD, ROR2, SNORA84, SPTLC1, SYK, ZNF484
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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