A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352958



Internal ID22265616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101052715..101053347hg38UCSC Ensembl
chr10:102812472..102813104hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215105
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352958
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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