A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557009



Internal ID18855290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5696474..5744316hg38UCSC Ensembl
Innerchr16:5746475..5794317hg19UCSC Ensembl
Innerchr16:5686476..5734318hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3847843
hg1947843
hg1847843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049616
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557009
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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