A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769515



Internal ID19311127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46192466..46192795hg38UCSC Ensembl
chr21:47612380..47612709hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072611
Supporting Variants
SamplesKWP1
Known GenesLSS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769515
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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