A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623151



Internal ID21815198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3926663..3939857hg38UCSC Ensembl
chr19:3926661..3939855hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813195
hg1913195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052411
Supporting Variants
Samples
Known GenesATCAY, NMRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623151
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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