A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150471



Internal ID18848507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86074..373358hg38UCSC Ensembl
Outerchr4:85965..367147hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38287285
hg19281183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003772
SamplesKWB1
Known GenesZNF141, ZNF595, ZNF718, ZNF732, ZNF876P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150471
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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