A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044232



Internal ID18786763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46176448..46313699hg38UCSC Ensembl
Innerchr10:47547684..47684935hg19UCSC Ensembl
Innerchr10:47017690..47154941hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38137252
hg19137252
hg18137252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3706806
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)nsv1044232
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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