A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522976



Internal ID15450269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15068559..15278848hg38UCSC Ensembl
Innerchr7:15108184..15318473hg19UCSC Ensembl
Innerchr7:15074709..15284998hg18UCSC Ensembl
Innerchr7:14881424..15091713hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38210290
hg19210290
hg18210290
hg17210290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698646
Samples
Known GenesAGMO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522976
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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