A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573837



Internal ID16361246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907804..89908560hg38UCSC Ensembl
Innerchr16:89974212..89974968hg19UCSC Ensembl
Innerchr16:88501713..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5341n54
Supporting Variantsnssv864011, nssv864016, nssv864018, nssv864012, nssv864013, nssv864014, nssv864015, nssv864017
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573837
Frequency
Sample Size17421
Observed Gain4
Observed Loss4
Observed Complex0
Frequencyn/a


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