A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156790



Internal ID22087191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159321255..159367158hg38UCSC Ensembl
Outerchr1:159318338..159370191hg38UCSC Ensembl
Innerchr1:159291045..159336948hg19UCSC Ensembl
Outerchr1:159288128..159339981hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3851854
hg1951854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022960
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156790
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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