A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592663



Internal ID16380072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183824938..183825871hg38UCSC Ensembl
Innerchr3:183542726..183543659hg19UCSC Ensembl
Innerchr3:185025420..185026353hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38934
hg19934
hg18934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982567
Samples
Known GenesMAP6D1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592663
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