A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329757



Internal ID22263706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158102504..158102504hg38UCSC Ensembl
chr6:158523536..158523536hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564557
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329757
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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