A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852347



Internal ID15799617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5615455..5678903hg38UCSC Ensembl
Innerchr16:5665456..5728904hg19UCSC Ensembl
Innerchr16:5605457..5668905hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3863449
hg1963449
hg1863449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571309
Supporting Variants
Samples
Known GenesMIR8065
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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