A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573589



Internal ID16014312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88530296..88534196hg38UCSC Ensembl
Innerchr16:88596704..88600604hg19UCSC Ensembl
Innerchr16:87124205..87128105hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383901
hg193901
hg183901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862561
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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