A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570957



Internal ID16358366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:380011..441405hg38UCSC Ensembl
Innerchr16:430011..491405hg19UCSC Ensembl
Innerchr16:370012..431406hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3861395
hg1961395
hg1861395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4810n54
Supporting Variantsnssv851310
Samples
Known GenesDECR2, LOC100134368, NME4, RAB11FIP3, TMEM8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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