A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008804



Internal ID19098022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22047014..22072911hg38UCSC Ensembl
Innerchr4:22048637..22074534hg19UCSC Ensembl
Innerchr4:21657735..21683632hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3825898
hg1925898
hg1825898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5155n100
Supporting Variantsnssv3620573, nssv3737752, nssv3620574
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)nsv1008804
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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