A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259211



Internal ID20468429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053705..12066581hg38UCSC Ensembl
chr19:12164520..12177396hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812877
hg1912877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743634
Supporting Variants
Samples
Known GenesZNF844
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259211
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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