A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355176



Internal ID22234961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122669200..122669291hg38UCSC Ensembl
chr10:124428716..124428807hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224539
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355176
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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