A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935504



Internal ID22710847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85002708..85010895hg38UCSC Ensembl
chr16:85036314..85044501hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg388188
hg198188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378974
Samples
Known GenesZDHHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935504
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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