A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938664



Internal ID22714047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11717638..11718007hg38UCSC Ensembl
chr16:11811494..11811863hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386017
Samples
Known GenesTXNDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938664
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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