A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063199



Internal ID19152418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79224428..79248434hg38UCSC Ensembl
Innerchr16:79258325..79282331hg19UCSC Ensembl
Innerchr16:77815826..77839832hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824007
hg1924007
hg1824007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559770
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)nsv1063199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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