A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013037



Internal ID19102255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128662394..128702740hg38UCSC Ensembl
Innerchr3:128381237..128421583hg19UCSC Ensembl
Innerchr3:129863927..129904273hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3840347
hg1940347
hg1840347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4857n100
Supporting Variantsnssv3603519, nssv3603517, nssv3736419, nssv3736418, nssv3736417, nssv3603518
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)nsv1013037
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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