A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149302



Internal ID18856574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:138045053..138046054hg38UCSC Ensembl
Outerchr4:138966207..138967208hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002813
SamplesKWB1
Known GenesLINC00616
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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