A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579014



Internal ID18877295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23748491..23837800hg38UCSC Ensembl
Innerchr2:23971361..24060670hg19UCSC Ensembl
Innerchr2:23824865..23914174hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3889310
hg1989310
hg1889310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014398
Supporting Variants
Samples
Known GenesATAD2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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