A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329781



Internal ID22264179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12013090..12013350hg38UCSC Ensembl
chr10:12055089..12055349hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215897
Supporting Variants
SamplesNA19238
Known GenesUPF2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329781
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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