A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769120



Internal ID19304829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8763951..8764023hg38UCSC Ensembl
chr21:9652784..9652856hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072139
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769120
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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