A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049205



Internal ID19138424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19935610..19962546hg38UCSC Ensembl
Innerchr16:19946932..19973868hg19UCSC Ensembl
Innerchr16:19854433..19881369hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3826937
hg1926937
hg1826937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3547055
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)nsv1049205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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