A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928821



Internal ID22704066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16314497..16331261hg38UCSC Ensembl
chr19:16425308..16442072hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3816765
hg1916765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391176
Samples
Known GenesKLF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928821
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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