A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038833



Internal ID19128052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19933041..19959991hg38UCSC Ensembl
Innerchr16:19944363..19971313hg19UCSC Ensembl
Innerchr16:19851864..19878814hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3826951
hg1926951
hg1826951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3542922
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)nsv1038833
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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