A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008773



Internal ID18751304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86198995..86217612hg38UCSC Ensembl
Innerchr4:87120148..87138765hg19UCSC Ensembl
Innerchr4:87339172..87357789hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3818618
hg1918618
hg1818618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633921
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)nsv1008773
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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