A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1024128



Internal ID15971398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8757929..9209719hg38UCSC Ensembl
Innerchr5:8758041..9209831hg19UCSC Ensembl
Innerchr5:8811041..9262831hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38451791
hg19451791
hg18451791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597069
Supporting Variants
Samples
Known GenesMIR4636, SEMA5A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1024128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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