A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260505



Internal ID20469723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19572160..19572255hg38UCSC Ensembl
chr19:19682969..19683064hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749220
Supporting Variants
Samples
Known GenesPBX4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260505
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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