A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602963



Internal ID16390372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39082608..39095214hg38UCSC Ensembl
Innerchr6:39050384..39062990hg19UCSC Ensembl
Innerchr6:39158362..39170968hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3812607
hg1912607
hg1812607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154308
Samples1780854065_A
Known GenesGLP1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer