A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550798



Internal ID15991521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46306562..46379219hg38UCSC Ensembl
Innerchr10:47677798..47750479hg19UCSC Ensembl
Innerchr10:47147804..47220485hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3872658
hg1972682
hg1872682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1119n54
Supporting Variantsnssv747638
Samples
Known GenesANTXRL, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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