A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524901



Internal ID18823182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109628262..109687461hg38UCSC Ensembl
Innerchr12:110066067..110125266hg19UCSC Ensembl
Innerchr12:108550450..108609649hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3859200
hg1959200
hg1859200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047385
Supporting Variants
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)nssv3524901
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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