A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040780



Internal ID19129999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28883965..28971225hg38UCSC Ensembl
Innerchr10:29172894..29260154hg19UCSC Ensembl
Innerchr10:29212900..29300160hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3887261
hg1987261
hg1887261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv698n100
Supporting Variantsnssv3506169
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)nsv1040780
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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