A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712434



Internal ID19010715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:34007089..34701551hg38UCSC Ensembl
Innerchr12:34160024..34854486hg19UCSC Ensembl
Innerchr12:34051291..34745753hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38694463
hg19694463
hg18694463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036399
Supporting Variants
Samples
Known GenesALG10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712434
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