A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152666



Internal ID18852654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:95045804..95045880hg38UCSC Ensembl
Outerchr1:95511360..95511436hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999851
SamplesKWB1
Known GenesALG14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152666
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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