A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327493



Internal ID22267014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13781227..13781752hg38UCSC Ensembl
chr6:13781459..13781984hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198565
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327493
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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