A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704817



Internal ID15094783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88398104..88488151hg38UCSC Ensembl
Innerchr16:88464512..88554559hg19UCSC Ensembl
Innerchr16:86992013..87082060hg18UCSC Ensembl
Innerchr16:86992013..87082060hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3890048
hg1990048
hg1890048
hg1790048
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528251
Supporting Variants
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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