A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581699



Internal ID18879980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52173006..52358136hg38UCSC Ensembl
Innerchr2:52400144..52585274hg19UCSC Ensembl
Innerchr2:52253648..52438778hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38185131
hg19185131
hg18185131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3581699
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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