A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005919



Internal ID19095137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44963167..45004306hg38UCSC Ensembl
Innerchr4:44965184..45006323hg19UCSC Ensembl
Innerchr4:44659941..44701080hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3841140
hg1941140
hg1841140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3625058
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005919
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