A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736592



Internal ID20512542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57680049..57680108hg38UCSC Ensembl
chr16:57713961..57714020hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267894
Samples
Known GenesGPR97
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736592
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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