A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511085



Internal ID20884410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84400601..84559200hg38UCSC Ensembl
chr16:84434207..84592806hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38158600
hg19158600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2953n223
Supporting Variantsnssv18032997
Samples
Known GenesATP2C2, TLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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