A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368897



Internal ID22123078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41003395..41003533hg38UCSC Ensembl
chr13:41577531..41577669hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528136
Supporting Variants
SamplesHG00512
Known GenesELF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368897
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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