A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604579



Internal ID16391988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123275447..123357056hg38UCSC Ensembl
Innerchr6:123596592..123678201hg19UCSC Ensembl
Innerchr6:123638291..123719900hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3881610
hg1981610
hg1881610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072367
Samples
Known GenesTRDN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604579
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