A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515344



Internal ID18813625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:45001..97515hg38UCSC Ensembl
Innerchr12:150430..206681hg19UCSC Ensembl
Innerchr12:20691..76942hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3852515
hg1956252
hg1856252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035999
Supporting Variants
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515344
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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