A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2844n106



Internal ID20162201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86055209..86058847hg38UCSC Ensembl
chr4:86976362..86980000hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383639
hg193639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120834, nsv1111814, nsv1121296
SamplesKWS2
Known GenesMAPK10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2844n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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