A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010855



Internal ID19100072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4158085..4175965hg38UCSC Ensembl
Innerchr2:4205675..4223555hg19UCSC Ensembl
Innerchr2:4183550..4201430hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3817881
hg1917881
hg1817881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3571356, nssv3571357
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)nsv1010855
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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