A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517384



Internal ID18815665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9477948..9587658hg38UCSC Ensembl
Innerchr12:9630544..9740254hg19UCSC Ensembl
Innerchr12:9521811..9631521hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38109711
hg19109711
hg18109711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050850
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)nssv3517384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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