A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3727989



Internal ID18679584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24907673..25349661hg38UCSC Ensembl
Innerchr2:25130542..25572530hg19UCSC Ensembl
Innerchr2:24984046..25426034hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38441989
hg19441989
hg18441989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008732
Supporting Variants
Samples
Known GenesADCY3, DNAJC27, DNAJC27-AS1, DNMT3A, EFR3B, MIR1301, POMC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3727989
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