A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604485



Internal ID16045208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109638066..109733283hg38UCSC Ensembl
Innerchr6:109959269..110054486hg19UCSC Ensembl
Innerchr6:110065962..110161179hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3895218
hg1995218
hg1895218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071962
Samples
Known GenesAK9, FIG4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604485
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