A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550762



Internal ID15991485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46393582hg38UCSC Ensembl
Innerchr10:47543322..47764834hg19UCSC Ensembl
Innerchr10:47013328..47234840hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38221497
hg19221513
hg18221513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1110n54
Supporting Variantsnssv747536
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)nsv550762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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