A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155718



Internal ID22086223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52601975..52666361hg38UCSC Ensembl
Outerchr2:52600249..52669328hg38UCSC Ensembl
Innerchr2:52829113..52893499hg19UCSC Ensembl
Outerchr2:52827387..52896466hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3869080
hg1969080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011342
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155718
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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