A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977428



Internal ID19242049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45635086..45637686hg38UCSC Ensembl
Outerchr21:47055000..47057600hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115619
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977428
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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