A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738421



Internal ID20514389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10071983..10072044hg38UCSC Ensembl
chr19:10182659..10182720hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258897
Samples
Known GenesC3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738421
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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