A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153630



Internal ID18854266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:5856900..5856983hg38UCSC Ensembl
Outerchr4:5858627..5858710hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002285
SamplesKWB1
Known GenesCRMP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153630
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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