A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14310279



Internal ID22257509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194311184..194311184hg38UCSC Ensembl
chr3:194028973..194028973hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3562763
Supporting Variants
SamplesNA19238
Known GenesLINC00887
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14310279
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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