A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3708086



Internal ID19006367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7818125..7978362hg38UCSC Ensembl
Innerchr12:7970721..8130958hg19UCSC Ensembl
Innerchr12:7861988..8022225hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38160238
hg19160238
hg18160238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041719
Supporting Variants
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3708086
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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