A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528680



Internal ID6024110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103807720..103832927hg19UCSC Ensembl
Innerchr4:104027155..104052376hg18UCSC Ensembl
Innerchr4:104165310..104190531hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv705321
Samples
Known GenesCISD2, SLC9B1
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv528680
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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