A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128107



Internal ID18932800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165422291..165422354hg38UCSC Ensembl
Outerchr4:166343443..166343506hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957559
SamplesKWS1
Known GenesCPE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128107
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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