A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999739



Internal ID19159275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119012086..119101798hg38UCSC Ensembl
Innerchr3:118730933..118820645hg19UCSC Ensembl
Innerchr3:120213623..120303335hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3889713
hg1989713
hg1889713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4844n100
Supporting Variantsnssv3735271, nssv3604491, nssv3735275, nssv3735270, nssv3735273, nssv3735274, nssv3735272
Samples
Known GenesIGSF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999739
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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