A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582653



Internal ID16370062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:109380824..109414508hg38UCSC Ensembl
Innerchr2:109997280..110030964hg19UCSC Ensembl
Innerchr2:109363712..109397396hg18UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3833685
hg1933685
hg1833685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916028
Samples
Known GenesSH3RF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582653
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