A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571402



Internal ID16358811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8271221..8286999hg38UCSC Ensembl
Innerchr16:8321223..8337001hg19UCSC Ensembl
Innerchr16:8261224..8277002hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3815779
hg1915779
hg1815779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852423, nssv852422
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571402
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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