A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011713



Internal ID19100931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055226..86070837hg38UCSC Ensembl
Innerchr4:86976379..86991990hg19UCSC Ensembl
Innerchr4:87195403..87211014hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3815612
hg1915612
hg1815612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n100
Supporting Variantsnssv3633919, nssv3633920
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)nsv1011713
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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