A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045995



Internal ID18788526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3356516..3424504hg38UCSC Ensembl
Innerchr16:3406516..3474504hg19UCSC Ensembl
Innerchr16:3346517..3414505hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3867989
hg1967989
hg1867989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2695n100
Supporting Variantsnssv3556965
Samples
Known GenesMTRNR2L4, OR2C1, ZNF174, ZSCAN32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045995
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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