A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550759



Internal ID15991482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46379901hg38UCSC Ensembl
Innerchr10:47543322..47751161hg19UCSC Ensembl
Innerchr10:47013328..47221167hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38207816
hg19207840
hg18207840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1110n54
Supporting Variantsnssv747532
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)nsv550759
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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