A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15185335



Internal ID21324144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119525206..119525206hg38UCSC Ensembl
chr2:120282782..120282782hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949756
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15185335
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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