A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004688



Internal ID18747219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86049077..86062079hg38UCSC Ensembl
Innerchr4:86970230..86983232hg19UCSC Ensembl
Innerchr4:87189254..87202256hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3813003
hg1913003
hg1813003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5332n100
Supporting Variantsnssv3633906
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)nsv1004688
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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