A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523660



Internal ID18821941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:61394986..61436589hg38UCSC Ensembl
Innerchr12:61788767..61830370hg19UCSC Ensembl
Innerchr12:60075034..60116637hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3841604
hg1941604
hg1841604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038629
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)nssv3523660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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