A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056126



Internal ID18798657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47624794..47704744hg38UCSC Ensembl
Innerchr16:47658705..47738655hg19UCSC Ensembl
Innerchr16:46216206..46296156hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3879951
hg1979951
hg1879951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722703
Samples
Known GenesPHKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056126
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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