A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729801



Internal ID19028082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88848330..89002373hg38UCSC Ensembl
Innerchr2:89147843..89301870hg19UCSC Ensembl
Innerchr2:88928958..89082985hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38154044
hg19154028
hg18154028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012148
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)nssv3729801
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