A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528286



Internal ID15108893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39051727..39092702hg38UCSC Ensembl
Innerchr6:39019503..39060478hg19UCSC Ensembl
Innerchr6:39127481..39168456hg18UCSC Ensembl
Innerchr6:39127481..39168456hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3840976
hg1940976
hg1840976
hg1740976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704856
Samples
Known GenesGLP1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528286
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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