A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327562



Internal ID22261282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266086..16266161hg38UCSC Ensembl
chr6:16266317..16266392hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527510
Supporting Variants
SamplesNA19238
Known GenesGMPR
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327562
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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