A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152155



Internal ID18853295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42258021..42258173hg38UCSC Ensembl
Outerchr21:43678131..43678283hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996760
SamplesKWB1
Known GenesABCG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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