A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550736



Internal ID15991459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46377652hg38UCSC Ensembl
Innerchr10:47537368..47748912hg19UCSC Ensembl
Innerchr10:47007374..47218918hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38211521
hg19211545
hg18211545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1110n54
Supporting Variantsnssv747393, nssv747394
Samples
Known GenesANTXRL, ANTXRLP1, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550736
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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