A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748161



Internal ID20524186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30130688..30130778hg38UCSC Ensembl
chr19:30621595..30621685hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748161
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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