A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851308



Internal ID15798578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:347044..451362hg38UCSC Ensembl
Innerchr16:397044..501362hg19UCSC Ensembl
Innerchr16:337045..441363hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38104319
hg19104319
hg18104319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570955
Supporting Variants
Samples
Known GenesAXIN1, DECR2, 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)nssv851308
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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