A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768220



Internal ID18961032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10443483..10443543hg38UCSC Ensembl
chr21:11068914..11068974hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073110
Supporting Variants
SamplesKWP1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768220
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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