A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128839



Internal ID19266859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8987967..9077467hg38UCSC Ensembl
Outerchr21:9826800..9916300hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3889501
hg1989501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2303n106
Supporting Variantsnssv3961507
SamplesKWS1
Known GenesTEKT4P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128839
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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