A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573605



Internal ID16014328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533696..88547211hg38UCSC Ensembl
Innerchr16:88600104..88613619hg19UCSC Ensembl
Innerchr16:87127605..87141120hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3813516
hg1913516
hg1813516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5298n54
Supporting Variantsnssv862587
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573605
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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