A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956395



Internal ID16958582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86145216..86145377hg38UCSC Ensembl
Outerchr4:87066369..87066530hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005254
SamplesBILGI_BIOE
Known GenesMAPK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956395
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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