A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522907



Internal ID18821188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37620204..38037452hg38UCSC Ensembl
Innerchr12:38014006..38431254hg19UCSC Ensembl
Innerchr12:36300273..36717521hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38417249
hg19417249
hg18417249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044076
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)nssv3522907
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