A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769753



Internal ID19308007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39109756..39111857hg38UCSC Ensembl
chr20:37738399..37740500hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073058
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769753
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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