A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515355



Internal ID20888714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84024388..84236392hg38UCSC Ensembl
chr16:84057993..84269998hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38212005
hg19212006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2952n223
Supporting Variantsnssv18032941
Samples
Known GenesADAD2, DNAAF1, HSDL1, KCNG4, MBTPS1, SLC38A8, TAF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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