A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559259



Internal ID18857540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:51725226..51745916hg38UCSC Ensembl
Innerchr16:51759137..51779827hg19UCSC Ensembl
Innerchr16:50316638..50337328hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3820691
hg1920691
hg1820691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058226
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)nssv3559259
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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