A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603440



Internal ID16390849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65427367..65504920hg38UCSC Ensembl
Innerchr6:66137260..66214813hg19UCSC Ensembl
Innerchr6:66193981..66271534hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3877554
hg1977554
hg1877554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10727n54
Supporting Variantsnssv1062635
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603440
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