A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522859



Internal ID18821140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37463949..37593912hg38UCSC Ensembl
Innerchr12:37857751..37987714hg19UCSC Ensembl
Innerchr12:36144018..36273981hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38129964
hg19129964
hg18129964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048872
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)nssv3522859
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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