A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523110



Internal ID15450403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135267703..135268257hg38UCSC Ensembl
Innerchr7:134952455..134953009hg19UCSC Ensembl
Innerchr7:134602995..134603549hg18UCSC Ensembl
Innerchr7:134409710..134410264hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
hg17555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698807
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523110
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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