A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751661



Internal ID21387496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2926377..2929306hg38UCSC Ensembl
chr19:2926375..2929304hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432802
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751661
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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