A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583014



Internal ID18881295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168414178..168440571hg38UCSC Ensembl
Innerchr2:169270688..169297081hg19UCSC Ensembl
Innerchr2:168978934..169005327hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3826394
hg1926394
hg1826394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001292
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)nssv3583014
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