A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963277



Internal ID18884390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86055209..86058794hg38UCSC Ensembl
Outerchr4:86976362..86979947hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383586
hg193586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120834
Supporting Variants
SamplesKWS2
Known GenesMAPK10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963277
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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