A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039953



Internal ID18782484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46370859hg38UCSC Ensembl
Innerchr10:47541177..47742076hg19UCSC Ensembl
Innerchr10:47011183..47212082hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38200919
hg19200900
hg18200900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv837n100
Supporting Variantsnssv3510488
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039953
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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