A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155820



Internal ID22086325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:48358484..48482405hg38UCSC Ensembl
Outerchr1:48354622..48497431hg38UCSC Ensembl
Innerchr1:48824156..48948077hg19UCSC Ensembl
Outerchr1:48820294..48963103hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38142810
hg19142810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015236
Samples
Known GenesSPATA6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155820
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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