A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013874



Internal ID19103093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35675889..35715858hg38UCSC Ensembl
Innerchr4:35677511..35717480hg19UCSC Ensembl
Innerchr4:35353906..35393875hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3839970
hg1939970
hg1839970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5191n100
Supporting Variantsnssv3625023, nssv3739346, nssv3625025, nssv3625022, nssv3739347, nssv3739345, nssv3625024
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)nsv1013874
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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