A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327559



Internal ID22316971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16128346..16132370hg38UCSC Ensembl
chr6:16128577..16132601hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204328
Supporting Variants
SamplesNA19240
Known GenesMYLIP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327559
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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