A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260183



Internal ID20469401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2643289..2643289hg38UCSC Ensembl
chr19:2643287..2643287hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766800
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260183
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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