A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604317



Internal ID16391726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101636616..101717454hg38UCSC Ensembl
Innerchr6:102084491..102165329hg19UCSC Ensembl
Innerchr6:102191184..102272022hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3880839
hg1980839
hg1880839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070793
Samples
Known GenesGRIK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604317
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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