A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772679



Internal ID18962112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743018..43743719hg38UCSC Ensembl
chr21:45162899..45163600hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072187
Supporting Variants
SamplesKWP1
Known GenesPDXK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772679
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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