A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039990



Internal ID18782521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46174643..46333389hg38UCSC Ensembl
Innerchr10:47545879..47704625hg19UCSC Ensembl
Innerchr10:47015885..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158747
hg19158747
hg18158747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3508209, nssv3521742
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)nsv1039990
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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