A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571303



Internal ID18869584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3838382..3876759hg38UCSC Ensembl
Innerchr2:3885972..3924349hg19UCSC Ensembl
Innerchr2:3863847..3902224hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005377
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)nssv3571303
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