A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042608



Internal ID18785139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46176448..46329229hg38UCSC Ensembl
Innerchr10:47547684..47700465hg19UCSC Ensembl
Innerchr10:47017690..47170471hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38152782
hg19152782
hg18152782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3520955, nssv3706807
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)nsv1042608
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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