A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352954



Internal ID22265613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100472075..100472268hg38UCSC Ensembl
chr10:102231832..102232025hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222450
Supporting Variants
SamplesNA19238
Known GenesWNT8B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352954
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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