A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111814



Internal ID18938570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86055247..86058847hg38UCSC Ensembl
Outerchr4:86976400..86980000hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n106
Supporting Variantsnssv3964725
SamplesKWS2
Known GenesMAPK10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111814
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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