A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040839



Internal ID18783370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11361749..11384988hg38UCSC Ensembl
Innerchr16:11455606..11478845hg19UCSC Ensembl
Innerchr16:11363107..11386346hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3823240
hg1923240
hg1823240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557135
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)nsv1040839
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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