A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946586



Internal ID22722079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51339840..51339894hg38UCSC Ensembl
chr19:51843094..51843148hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396551
Samples
Known GenesVSIG10L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946586
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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