A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034355



Internal ID15887541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64399566..64405404hg38UCSC Ensembl
Innerchr5:63695393..63701231hg19UCSC Ensembl
Innerchr5:63731149..63736987hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385839
hg195839
hg185839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1034355
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