A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508154



Internal ID18459749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46289800hg38UCSC Ensembl
Innerchr10:47541177..47661036hg19UCSC Ensembl
Innerchr10:47011183..47131042hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119860
hg19119860
hg18119860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048652
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508154
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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