A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014398



Internal ID19103617
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 StatusM
Merged Variantsdgv3741n100
Supporting Variantsnssv3579014
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)nsv1014398
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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