A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573600



Internal ID16014323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533643..88534417hg38UCSC Ensembl
Innerchr16:88600051..88600825hg19UCSC Ensembl
Innerchr16:87127552..87128326hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38775
hg19775
hg18775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5297n54
Supporting Variantsnssv862577
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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