A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155753



Internal ID22086258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87134049..87189966hg38UCSC Ensembl
Outerchr2:87117615..87192772hg38UCSC Ensembl
Innerchr2:87361172..87417089hg19UCSC Ensembl
Outerchr2:87344738..87419895hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3875158
hg1975158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n97
Supporting Variantsnssv4011360
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155753
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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