A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150038



Internal ID18855889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10419889..10422679hg38UCSC Ensembl
Outerchr21:11089778..11092568hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg382791
hg192791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998826
SamplesKWB1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150038
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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