A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028848



Internal ID15882034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29418097..29461866hg38UCSC Ensembl
Innerchr5:29418204..29461973hg19UCSC Ensembl
Innerchr5:29453961..29497730hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3843770
hg1943770
hg1843770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597755
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)nssv1028848
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