A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570954



Internal ID16011677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:342461..530124hg38UCSC Ensembl
Innerchr16:392461..580124hg19UCSC Ensembl
Innerchr16:332462..520125hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38187664
hg19187664
hg18187664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851307
Samples
Known GenesAXIN1, CAPN15, DECR2, LINC00235, LOC100134368, MRPL28, NME4, RAB11FIP3, TMEM8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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