A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036241



Internal ID18778772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5271882..5387609hg38UCSC Ensembl
Innerchr16:5321883..5437610hg19UCSC Ensembl
Innerchr16:5261884..5377611hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38115728
hg19115728
hg18115728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556993
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)nsv1036241
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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