A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604456



Internal ID16391865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107999992..108043747hg38UCSC Ensembl
Innerchr6:108321196..108364951hg19UCSC Ensembl
Innerchr6:108427889..108471644hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3843756
hg1943756
hg1843756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071907
Samples
Known GenesOSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604456
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