A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153928



Internal ID15853689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:51869013..51903238hg38UCSC Ensembl
Innerchr5:51164847..51199072hg19UCSC Ensembl
Innerchr5:51200604..51234829hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3834226
hg1934226
hg1834226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598145
Supporting Variants
Samples1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153928
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