A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145826



Internal ID19203322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:21253489..21256171hg38UCSC Ensembl
Outerchr20:21234127..21236809hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382683
hg192683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997183
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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