A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522664



Internal ID15449957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53808969..53811086hg38UCSC Ensembl
Innerchr7:53876662..53878779hg19UCSC Ensembl
Innerchr7:53844156..53846273hg18UCSC Ensembl
Innerchr7:53650871..53652988hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg382118
hg192118
hg182118
hg172118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706066
Samples
Known GenesFLJ45974
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522664
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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