A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155914



Internal ID22086419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:211178951..211236973hg38UCSC Ensembl
Outerchr2:211176953..211237793hg38UCSC Ensembl
Innerchr2:212043676..212101698hg19UCSC Ensembl
Outerchr2:212041678..212102518hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3860841
hg1960841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016166
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155914
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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