A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851309



Internal ID15798579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:376432..437728hg38UCSC Ensembl
Innerchr16:426432..487728hg19UCSC Ensembl
Innerchr16:366433..427729hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3861297
hg1961297
hg1861297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570956
Supporting Variants
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)nssv851309
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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