A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062188



Internal ID19151407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24278606..24413936hg38UCSC Ensembl
Innerchr19:24461408..24596738hg19UCSC Ensembl
Innerchr19:24253248..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38135331
hg19135331
hg18135331
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3489n100
Supporting Variantsnssv3570735, nssv3570736, nssv3570733, nssv3570734
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)nsv1062188
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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