A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586218



Internal ID20959289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107936497..114408912hg38UCSC Ensembl
chr11:107807223..114279634hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386472416
hg196472412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235855
Samples
Known GenesACAT1, ALG9, ANKK1, ARHGAP20, ATM, BCO2, BTG4, C11orf1, C11orf52, C11orf53, C11orf57, C11orf65, C11orf71, C11orf87, C11orf88, CLDN25, COLCA1, COLCA2, CRYAB, CUL5, DDX10, DIXDC1, DLAT, DRD2, EXPH5, FDX1, FDXACB1, HSPB2, HSPB2-C11orf52, HTR3A, HTR3B, IL18, KDELC2, LAYN, LOC100132078, LOC387810, MIR34B, MIR34C, MIR4301, MIR4491, NCAM1, NCAM1-AS1, NNMT, NPAT, PIH1D2, PLET1, POU2AF1, PPP2R1B, PTS, RAB39A, RBM7, RDX, SDHD, SIK2, TEX12, TIMM8B, TMPRSS5, TTC12, USP28, ZBTB16, ZC3H12C, ZW10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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