A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408630



Internal ID22466500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9606524..9606524hg38UCSC Ensembl
chr19:9717200..9717200hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408630
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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