A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038083



Internal ID18780614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46307201hg38UCSC Ensembl
Innerchr10:47541177..47678437hg19UCSC Ensembl
Innerchr10:47011183..47148443hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38137261
hg19137261
hg18137261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3506365, nssv3520983
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)nsv1038083
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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