A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377865



Internal ID22167663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84997284..84997895hg38UCSC Ensembl
chr16:85030890..85031501hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219364
Supporting Variants
SamplesHG00514
Known GenesZDHHC7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377865
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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