A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038301



Internal ID18780832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46281263hg38UCSC Ensembl
Innerchr10:47541177..47652499hg19UCSC Ensembl
Innerchr10:47011183..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38111323
hg19111323
hg18111323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831n100
Supporting Variantsnssv3516441, nssv3502958, nssv3518276, nssv3518963, nssv3511435
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)nsv1038301
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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