A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352940



Internal ID22265528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100376101..100376167hg38UCSC Ensembl
chr10:102135858..102135924hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221185
Supporting Variants
SamplesNA19238
Known GenesLINC00263
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352940
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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