A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526101



Internal ID18477696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:123634608..123688184hg38UCSC Ensembl
Innerchr12:124119155..124172731hg19UCSC Ensembl
Innerchr12:122685108..122738684hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3853577
hg1953577
hg1853577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053101
Supporting Variants
Samples
Known GenesGTF2H3, TCTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526101
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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