A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038320



Internal ID18780851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12923630..12949595hg38UCSC Ensembl
Innerchr16:13017487..13043452hg19UCSC Ensembl
Innerchr16:12924988..12950953hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3825966
hg1925966
hg1825966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718887
Samples
Known GenesSHISA9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038320
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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