A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524928



Internal ID6018679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150731698..150766799hg19UCSC Ensembl
Innerchr7:150362631..150397732hg18UCSC Ensembl
Innerchr7:150169346..150204447hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv700941
Samples
Known GenesABCB8, ACCN3, CDK5, SLC4A2
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)nsv524928
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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