A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933004



Internal ID22708311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12013039..12013531hg38UCSC Ensembl
chr16:12106896..12107388hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389179
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933004
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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