A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503216



Internal ID18801497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33246118..33546428hg38UCSC Ensembl
Innerchr12:33399053..33699363hg19UCSC Ensembl
Innerchr12:33290320..33590630hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38300311
hg19300311
hg18300311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035988
Supporting Variants
Samples
Known GenesSYT10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503216
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer