A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937395



Internal ID21357464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12943310..12943365hg38UCSC Ensembl
chr16:13037167..13037222hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184198
SamplesHG002
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937395
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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