A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597079



Internal ID16384488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9545589..9546300hg38UCSC Ensembl
Innerchr5:9545701..9546412hg19UCSC Ensembl
Innerchr5:9598701..9599412hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38712
hg19712
hg18712
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9573n54
Supporting Variantsnssv1024146, nssv1024143, nssv1024145, nssv1024144
Samples
Known GenesSEMA5A, SNHG18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597079
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer