A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330347



Internal ID22286181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10427537..10432326hg38UCSC Ensembl
chr10:10469500..10474289hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384790
hg194790
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228501
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330347
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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