A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155921



Internal ID22086426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226478072..226481352hg38UCSC Ensembl
Outerchr2:226477322..226483083hg38UCSC Ensembl
Innerchr2:227342788..227346068hg19UCSC Ensembl
Outerchr2:227342038..227347799hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016186, nssv4016187
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155921
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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