A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155719



Internal ID22086224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52716652..52830900hg38UCSC Ensembl
Outerchr2:52712603..52831056hg38UCSC Ensembl
Innerchr2:52943790..53058038hg19UCSC Ensembl
Outerchr2:52939741..53058194hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38118454
hg19118454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169n97
Supporting Variantsnssv4011343
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155719
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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