A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204546



Internal ID21343349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735334..4735334hg38UCSC Ensembl
chr9:4735334..4735334hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950861
Supporting Variants
SamplesHG002
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204546
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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