A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718842



Internal ID18670437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6171275..6423196hg38UCSC Ensembl
Innerchr16:6221276..6473197hg19UCSC Ensembl
Innerchr16:6161277..6413198hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38251922
hg19251922
hg18251922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052728
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718842
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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