A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005338



Internal ID18747869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86102245..86187402hg38UCSC Ensembl
Innerchr4:87023398..87108555hg19UCSC Ensembl
Innerchr4:87242422..87327579hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3885158
hg1985158
hg1885158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742877
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)nsv1005338
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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