A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571703



Internal ID16359112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24527292..24532726hg38UCSC Ensembl
Innerchr16:24538613..24544047hg19UCSC Ensembl
Innerchr16:24446114..24451548hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385435
hg195435
hg185435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv854197
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571703
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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