A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518439



Internal ID15445732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136449517..136767335hg38UCSC Ensembl
Innerchr7:136134265..136452082hg19UCSC Ensembl
Innerchr7:135784805..136102622hg18UCSC Ensembl
Innerchr7:135591520..135909337hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38317819
hg19317818
hg18317818
hg17317818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695875
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518439
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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