A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571299



Internal ID18869580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3746245..3769098hg38UCSC Ensembl
Innerchr2:3793835..3816688hg19UCSC Ensembl
Innerchr2:3771710..3794563hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3822854
hg1922854
hg1822854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004469
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)nssv3571299
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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