A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024125



Internal ID19113342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7414033..7477796hg38UCSC Ensembl
Innerchr5:7414146..7477909hg19UCSC Ensembl
Innerchr5:7467146..7530909hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3863764
hg1963764
hg1863764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5562n100
Supporting Variantsnssv3639641
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024125
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