A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123777



Internal ID18925279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:39475023..39475077hg38UCSC Ensembl
Outerchr4:39476643..39476697hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973931
SamplesKWS2
Known GenesLIAS, MIR1273H
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123777
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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