A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571450



Internal ID16012173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10399260..10504610hg38UCSC Ensembl
Innerchr16:10493117..10598467hg19UCSC Ensembl
Innerchr16:10400618..10505968hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38105351
hg19105351
hg18105351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4907n54
Supporting Variantsnssv852526
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571450
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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