A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931412



Internal ID22706695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29036336..29040842hg38UCSC Ensembl
chr19:29527243..29531749hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384507
hg194507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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