A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977415



Internal ID19242269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8987967..9071067hg38UCSC Ensembl
Outerchr21:9826800..9909900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3883101
hg1983101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115605
Supporting Variants
SamplesKWS2
Known GenesTEKT4P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977415
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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