A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011890



Internal ID22073521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39380799..39431244hg38UCSC Ensembl
Outerchr18:39377776..39431781hg38UCSC Ensembl
Innerchr18:36960763..37011208hg19UCSC Ensembl
Outerchr18:36957740..37011745hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3854006
hg1954006
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155508
Supporting Variants
Samples
Known GenesLINC00669
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011890
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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