A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109619



Internal ID18906078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86264989..86265052hg38UCSC Ensembl
Outerchr4:87186142..87186205hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957145
SamplesKWS1
Known GenesMAPK10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109619
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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