A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354606



Internal ID22326313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114647208..114647362hg38UCSC Ensembl
chr10:116406967..116407121hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529447
Supporting Variants
SamplesNA19240
Known GenesABLIM1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354606
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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