A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2912740



Internal ID15387809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055343..86058719hg38UCSC Ensembl
Innerchr4:86976496..86979872hg19UCSC Ensembl
Innerchr4:87195520..87198896hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383377
hg193377
hg183377
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514230
Supporting Variants
SamplesNA19117
Known GenesMAPK10
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2912740
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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