A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623389



Internal ID21815436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3435851..3437714hg38UCSC Ensembl
chr19:3435849..3437712hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045998
Supporting Variants
Samples
Known GenesNFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623389
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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