A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154960



Internal ID22085465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241801257..241826297hg38UCSC Ensembl
Outerchr1:241800932..241828122hg38UCSC Ensembl
Innerchr1:241964559..241989599hg19UCSC Ensembl
Outerchr1:241964234..241991424hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3827191
hg1927191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007513
Samples
Known GenesWDR64
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154960
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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