A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147717



Internal ID19198627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:115007584..115010719hg38UCSC Ensembl
Outerchr4:115928740..115931875hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996506
SamplesKWB1
Known GenesNDST4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147717
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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