A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156327



Internal ID22084803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31274286..31276292hg38UCSC Ensembl
Outerchr5:31273870..31278657hg38UCSC Ensembl
Innerchr5:31274393..31276399hg19UCSC Ensembl
Outerchr5:31273977..31278764hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg384788
hg194788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020748
Samples
Known GenesCDH6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156327
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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