A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281619



Internal ID20848659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99955191..100728759hg38UCSC Ensembl
chr9:102717473..103491041hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38773569
hg19773569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558336
Supporting Variants
Samples
Known GenesERP44, INVS, MSANTD3, MSANTD3-TMEFF1, MURC, STX17, TEX10, TMEFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281619
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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