A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524611



Internal ID18476206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:71913836..72115561hg38UCSC Ensembl
Innerchr12:72307616..72509341hg19UCSC Ensembl
Innerchr12:70593883..70795608hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38201726
hg19201726
hg18201726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054578
Supporting Variants
Samples
Known GenesTBC1D15, TPH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524611
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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