A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633922



Internal ID18585517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86300327..86336300hg38UCSC Ensembl
Innerchr4:87221480..87257453hg19UCSC Ensembl
Innerchr4:87440504..87476477hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3835974
hg1935974
hg1835974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011494
Supporting Variants
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)nssv3633922
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