A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504854



Internal ID20878118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88604328..88604642hg38UCSC Ensembl
chr16:88670736..88671050hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033208
Samples
Known GenesZC3H18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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