A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154329



Internal ID22084834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:771719..874393hg38UCSC Ensembl
Outerchr1:690090..877938hg38UCSC Ensembl
Innerchr1:707099..809773hg19UCSC Ensembl
Outerchr1:625470..813318hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38187849
hg19187849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004840
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100133331, LOC100288069
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154329
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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