A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522305



Internal ID15102912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148771525..148811105hg38UCSC Ensembl
Innerchr7:148468617..148508197hg19UCSC Ensembl
Innerchr7:148099550..148139130hg18UCSC Ensembl
Innerchr7:147906265..147945845hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3839581
hg1939581
hg1839581
hg1739581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695087
Samples
Known GenesCUL1, EZH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522305
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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