A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354013



Internal ID22266624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71357111..71357297hg38UCSC Ensembl
chr10:73116868..73117054hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228660
Supporting Variants
SamplesNA19238
Known GenesSLC29A3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354013
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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