A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151660



Internal ID18853298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10325257..10494058hg38UCSC Ensembl
Outerchr21:11018399..11187200hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38168802
hg19168802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003082
SamplesKWB1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151660
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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