A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155211



Internal ID22085716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:31365571..31367831hg38UCSC Ensembl
Outerchr2:31363712..31368051hg38UCSC Ensembl
Innerchr2:31588437..31590697hg19UCSC Ensembl
Outerchr2:31586578..31590917hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg384340
hg194340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007609
Samples
Known GenesXDH
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155211
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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