A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013308



Internal ID18755839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86848541..86949016hg38UCSC Ensembl
Innerchr4:87769694..87870168hg19UCSC Ensembl
Innerchr4:87988718..88089192hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38100476
hg19100475
hg18100475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633924
Samples
Known GenesAFF1, C4orf36, LOC100506746, SLC10A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013308
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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