A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138997



Internal ID18905760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10403977..10415675hg38UCSC Ensembl
Outerchr21:11096782..11108480hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3811699
hg1911699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991609, nssv3986079
SamplesKWS1, KWS2
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138997
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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