A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550760



Internal ID16338169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46379977hg38UCSC Ensembl
Innerchr10:47543322..47751237hg19UCSC Ensembl
Innerchr10:47013328..47221243hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38207892
hg19207916
hg18207916
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112n54
Supporting Variantsnssv747534, nssv747533
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)nsv550760
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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