A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152215



Internal ID19198134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:141005765..141006087hg38UCSC Ensembl
Outerchr4:141926919..141927241hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996823
SamplesKWB1
Known GenesRNF150
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152215
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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