A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597302



Internal ID16384711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16179136..16179707hg38UCSC Ensembl
Innerchr5:16179245..16179816hg19UCSC Ensembl
Innerchr5:16232245..16232816hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38572
hg19572
hg18572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9621n54
Supporting Variantsnssv1026282
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597302
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