A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351726



Internal ID22311370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67643209..67753672hg38UCSC Ensembl
chr10:69402967..69513430hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38110464
hg19110464
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222449
Supporting Variants
SamplesNA19240
Known GenesCTNNA3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351726
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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