A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380586



Internal ID22438456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50405934..50412058hg38UCSC Ensembl
chr16:50439845..50445969hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg386125
hg196125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380586
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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