A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040358



Internal ID19129577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12543125..12556390hg38UCSC Ensembl
Innerchr16:12636982..12650247hg19UCSC Ensembl
Innerchr16:12544483..12557748hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3813266
hg1913266
hg1813266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557159
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040358
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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