A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327532



Internal ID22234198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15188177..15190593hg38UCSC Ensembl
chr6:15188408..15190824hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382417
hg192417
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529787
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327532
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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