A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524800



Internal ID18823081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:87593924..87669627hg38UCSC Ensembl
Innerchr12:87987701..88063404hg19UCSC Ensembl
Innerchr12:86511832..86587535hg18UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3875704
hg1975704
hg1875704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049734
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)nssv3524800
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