A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002641



Internal ID15949911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055260..86097335hg38UCSC Ensembl
Innerchr4:86976413..87018488hg19UCSC Ensembl
Innerchr4:87195437..87237512hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3842076
hg1942076
hg1842076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594761
Supporting Variants
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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