A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735994



Internal ID20511937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12943305..12943363hg38UCSC Ensembl
chr16:13037162..13037220hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265937
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735994
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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