A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937461



Internal ID22712829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2366983..2367090hg38UCSC Ensembl
chr16:2416984..2417091hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372852
Samples
Known GenesABCA17P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937461
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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