A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n21



Internal ID11600849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88382277..88503975hg38UCSC Ensembl
chr16:88448685..88570383hg19UCSC Ensembl
chr16:86976186..87097884hg18UCSC Ensembl
chr16:86976186..87097884hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38121699
hg19121699
hg18121699
hg17121699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528251, nsv521704
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv171n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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