A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240857



Internal ID20807897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83952013..85834110hg38UCSC Ensembl
chr16:83985618..85867716hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381882098
hg191882099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590742
Supporting Variants
Samples
Known GenesADAD2, ATP2C2, C16orf74, COTL1, COX4I1, CRISPLD2, DNAAF1, EMC8, FAM92B, GINS2, GSE1, HSDL1, KCNG4, KIAA0513, KLHL36, LINC00311, LOC400548, MBTPS1, MIR1910, MIR5093, MIR7851, NECAB2, OSGIN1, SLC38A8, TAF1C, TLDC1, USP10, WFDC1, ZDHHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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