A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102553



Internal ID22011786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18724785..21720303hg38UCSC Ensembl
chr19:18835595..21903105hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382995519
hg193067511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634421
Samples
Known GenesARMC6, ATP13A1, CERS1, CILP2, COMP, COPE, CRTC1, DDX49, GATAD2A, GDF1, GMIP, HAPLN4, HOMER3, LINC00663, LINC00664, LPAR2, MAU2, MEF2B, MEF2BNB, MEF2BNB-MEF2B, MIR1270-1, MIR1270-2, NCAN, NDUFA13, NR2C2AP, PBX4, RFXANK, SLC25A42, SUGP1, SUGP2, TM6SF2, TMEM161A, TSSK6, UPF1, YJEFN3, ZNF101, ZNF14, ZNF253, ZNF429, ZNF430, ZNF431, ZNF486, ZNF493, ZNF506, ZNF626, ZNF682, ZNF708, ZNF714, ZNF737, ZNF738, ZNF826P, ZNF85, ZNF90, ZNF93
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102553
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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