A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156307



Internal ID22084783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7177225..7189812hg38UCSC Ensembl
Outerchr5:7169363..7202522hg38UCSC Ensembl
Innerchr5:7177338..7189925hg19UCSC Ensembl
Outerchr5:7169476..7202635hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3833160
hg1933160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020626, nssv4020625
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156307
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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