A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074168



Internal ID18974942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38663278..38665279hg38UCSC Ensembl
chr4:38664899..38666900hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769344
SamplesKWP1
Known GenesFLJ13197, KLF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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