A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156426



Internal ID22086827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180951710..181006264hg38UCSC Ensembl
Outerchr5:180947523..181015400hg38UCSC Ensembl
Innerchr5:180378710..180433264hg19UCSC Ensembl
Outerchr5:180374523..180442400hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3867878
hg1967878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv238n97
Supporting Variantsnssv4018171, nssv4018172
Samples
Known GenesBTNL3, BTNL8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156426
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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