A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328238



Internal ID22195334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17526957..17527614hg38UCSC Ensembl
chr6:17527188..17527845hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191768
Supporting Variants
SamplesHG00731
Known GenesCAP2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328238
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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