A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355155



Internal ID22127690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122180043..122180410hg38UCSC Ensembl
chr10:123939558..123939925hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211110
Supporting Variants
SamplesHG00512
Known GenesTACC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355155
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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