A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328863



Internal ID22116822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7838906..7844549hg38UCSC Ensembl
chr10:7880869..7886512hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385644
hg195644
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228151
Supporting Variants
SamplesHG00512
Known GenesTAF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328863
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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