A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524853



Internal ID18476448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:99381747..99404400hg38UCSC Ensembl
Innerchr12:99775525..99798178hg19UCSC Ensembl
Innerchr12:98299656..98322309hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3822654
hg1922654
hg1822654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050331
Supporting Variants
Samples
Known GenesANKS1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524853
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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