A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152454



Internal ID15506544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051238..4094550hg38UCSC Ensembl
Innerchr3:4092922..4136234hg19UCSC Ensembl
Innerchr3:4067922..4111234hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843313
hg1943313
hg1843313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589422
Supporting Variants
Samples1780854016_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152454
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