A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14339265



Internal ID22262268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33907183..33907278hg38UCSC Ensembl
chr10:34196111..34196206hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527751
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14339265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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