A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572529



Internal ID16013252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46455924..46473704hg38UCSC Ensembl
Innerchr16:46489836..46507616hg19UCSC Ensembl
Innerchr16:45047337..45065117hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3817781
hg1917781
hg1817781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856641
Samples
Known GenesANKRD26P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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