A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155006



Internal ID22085511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20870300..20941822hg38UCSC Ensembl
Outerchr14:20867507..20945196hg38UCSC Ensembl
Innerchr14:21338459..21409981hg19UCSC Ensembl
Outerchr14:21335666..21413355hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3877690
hg1977690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009408
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155006
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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