A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519058



Internal ID15099665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8054974..8076164hg38UCSC Ensembl
Innerchr7:8094604..8115794hg19UCSC Ensembl
Innerchr7:8061129..8082319hg18UCSC Ensembl
Innerchr7:7867844..7889034hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3821191
hg1921191
hg1821191
hg1721191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696529
Samples
Known GenesGLCCI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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