A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14319429



Internal ID22260324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6661283..6661686hg38UCSC Ensembl
chr5:6661396..6661799hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194361
Supporting Variants
SamplesNA19238
Known GenesSRD5A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14319429
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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