A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191015



Internal ID21329874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188602164..188602164hg38UCSC Ensembl
chr3:188319952..188319952hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934504
Supporting Variants
SamplesHG002
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191015
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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