A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327595



Internal ID22234202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28273202..28273818hg38UCSC Ensembl
chr6:28240979..28241595hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198656
Supporting Variants
SamplesHG00733
Known GenesZSCAN26
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327595
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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