A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573019



Internal ID16013742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76238719..76284743hg38UCSC Ensembl
Innerchr16:76272617..76318640hg19UCSC Ensembl
Innerchr16:74830118..74876141hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3846025
hg1946024
hg1846024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5195n54
Supporting Variantsnssv859226
Samples
Known GenesCNTNAP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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