A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014691



Internal ID18757226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86054929..86065363hg38UCSC Ensembl
Innerchr4:86976082..86986516hg19UCSC Ensembl
Innerchr4:87195106..87205540hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3810435
hg1910435
hg1810435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633909
Samples
Known GenesMAPK10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014691
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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