A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288092



Internal ID20497310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42729328..42730275hg38UCSC Ensembl
chr5:42729430..42730377hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288092
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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