A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012098



Internal ID19101316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56006877..56021880hg38UCSC Ensembl
Innerchr3:56040905..56055908hg19UCSC Ensembl
Innerchr3:56015945..56030948hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3815004
hg1915004
hg1815004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593385
Samples
Known GenesERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012098
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