A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053082



Internal ID18795613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46274047hg38UCSC Ensembl
Innerchr10:47541177..47645283hg19UCSC Ensembl
Innerchr10:47011183..47115289hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38104107
hg19104107
hg18104107
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3517743, nssv3512421, nssv3504734, nssv3515232, nssv3522630, nssv3509375
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053082
Frequency
Sample Size29084
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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