A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040611



Internal ID19129830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121675623..121703845hg38UCSC Ensembl
Innerchr10:123435137..123463359hg19UCSC Ensembl
Innerchr10:123425127..123453349hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828223
hg1928223
hg1828223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3507813
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)nsv1040611
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