A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399170



Internal ID22457040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27250047..27260095hg38UCSC Ensembl
chr19:27740955..27751003hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3810049
hg1910049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399170
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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