A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626005



Internal ID21818052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7745899..7745899hg38UCSC Ensembl
chr19:7810785..7810785hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100820
Supporting Variants
Samples
Known GenesCD209
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626005
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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