A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355103



Internal ID22209610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120798394..120798510hg38UCSC Ensembl
chr10:122557906..122558022hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528145
Supporting Variants
SamplesHG00732
Known GenesMIR5694, WDR11-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355103
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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