A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138995



Internal ID18915756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10451060..10451112hg38UCSC Ensembl
Outerchr21:11061345..11061397hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991608, nssv3956100
SamplesKWS1, KWS2
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138995
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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