A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502168



Internal ID20875410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83829301..84247800hg38UCSC Ensembl
chr16:83862906..84281406hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38418500
hg19418501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032489
Samples
Known GenesADAD2, DNAAF1, HSDL1, KCNG4, MBTPS1, MLYCD, NECAB2, OSGIN1, SLC38A8, TAF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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