A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637476



Internal ID21829523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37297169..37311711hg38UCSC Ensembl
chr19:37788071..37802613hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3814543
hg1914543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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