A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593827



Internal ID16034550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24844879..24880230hg38UCSC Ensembl
Innerchr4:24846501..24881852hg19UCSC Ensembl
Innerchr4:24455599..24490950hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3835352
hg1935352
hg1835352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv994407
Samples
Known GenesCCDC149
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593827
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