A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018115



Internal ID22079746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180945168..180991103hg38UCSC Ensembl
Outerchr5:180934838..181006225hg38UCSC Ensembl
Innerchr5:180372168..180418103hg19UCSC Ensembl
Outerchr5:180361838..180433225hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3871388
hg1971388
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156422
Supporting Variants
Samples
Known GenesBTNL3, BTNL8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018115
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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