A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586840



Internal ID18885121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228468822..228491149hg38UCSC Ensembl
Innerchr2:229333538..229355865hg19UCSC Ensembl
Innerchr2:229041782..229064109hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3822328
hg1922328
hg1822328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012617
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)nssv3586840
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