A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527106



Internal ID15454399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78812471..78816092hg38UCSC Ensembl
Innerchr7:78441787..78445408hg19UCSC Ensembl
Innerchr7:78279723..78283344hg18UCSC Ensembl
Innerchr7:78086438..78090059hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383622
hg193622
hg183622
hg173622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703486
Samples
Known GenesMAGI2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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