A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586896



Internal ID18538491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:232384425..232406159hg38UCSC Ensembl
Innerchr2:233249135..233270869hg19UCSC Ensembl
Innerchr2:232957379..232979113hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3821735
hg1921735
hg1821735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006055
Supporting Variants
Samples
Known GenesECEL1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586896
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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