A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573838



Internal ID16014561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907859..89908560hg38UCSC Ensembl
Innerchr16:89974267..89974968hg19UCSC Ensembl
Innerchr16:88501768..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38702
hg19702
hg18702
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5341n54
Supporting Variantsnssv864019, nssv864021, nssv864020
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573838
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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