A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627925



Internal ID21819972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2872709..2872882hg38UCSC Ensembl
chr19:2872707..2872880hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043313
Supporting Variants
Samples
Known GenesZNF556
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627925
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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