A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594779



Internal ID16035502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86056924..86058774hg38UCSC Ensembl
Innerchr4:86978077..86979927hg19UCSC Ensembl
Innerchr4:87197101..87198951hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg381851
hg191851
hg181851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9149n54
Supporting Variantsnssv1002747, nssv1002748, nssv1002746, nssv1002749
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594779
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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