A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156375



Internal ID22086776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111573634..111575348hg38UCSC Ensembl
Outerchr5:111565528..111581474hg38UCSC Ensembl
Innerchr5:110909331..110911045hg19UCSC Ensembl
Outerchr5:110901226..110917171hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815947
hg1915946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018988, nssv4018989, nssv4018987
Samples
Known GenesSTARD4-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156375
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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