A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596262



Internal ID18894543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84668760..84718968hg38UCSC Ensembl
Innerchr3:84717911..84768119hg19UCSC Ensembl
Innerchr3:84800601..84850809hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3850209
hg1950209
hg1850209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013227
Supporting Variants
Samples
Known GenesLINC00971
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596262
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