A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571451



Internal ID16012174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10435543..10495488hg38UCSC Ensembl
Innerchr16:10529400..10589345hg19UCSC Ensembl
Innerchr16:10436901..10496846hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3859946
hg1959946
hg1859946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852527
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571451
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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