A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043915



Internal ID18786446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11091339..11108075hg38UCSC Ensembl
Innerchr16:11185196..11201932hg19UCSC Ensembl
Innerchr16:11092697..11109433hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3816737
hg1916737
hg1816737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557132
Samples
Known GenesCLEC16A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043915
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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