A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521704



Internal ID15102311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88382277..88503975hg38UCSC Ensembl
Innerchr16:88448685..88570383hg19UCSC Ensembl
Innerchr16:86976186..87097884hg18UCSC Ensembl
Innerchr16:86976186..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 Variantsdgv171n21
Supporting Variantsnssv698327
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521704
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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