A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999912



Internal ID18847738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101039007..101040032hg38UCSC Ensembl
Outerchr4:101960164..101961189hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152728
Supporting Variants
SamplesKWB1
Known GenesPPP3CA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999912
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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