A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135574



Internal ID18930279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10419918..10422695hg38UCSC Ensembl
Outerchr21:11089762..11092539hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg382778
hg192778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2353n106
Supporting Variantsnssv3964473, nssv3990067
SamplesKWS2, KWS1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135574
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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