A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762184



Internal ID18958392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33549893..33553894hg38UCSC Ensembl
chr21:34922199..34926200hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078502
Supporting Variants
SamplesKWP1
Known GenesMIR6501, SON
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762184
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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