A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138976



Internal ID19261678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10111580..10111796hg38UCSC Ensembl
Outerchr21:10589608..10589824hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991587
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138976
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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