A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550733



Internal ID15991456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46331115hg38UCSC Ensembl
Innerchr10:47537368..47702351hg19UCSC Ensembl
Innerchr10:47007374..47172357hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38164984
hg19164984
hg18164984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n54
Supporting Variantsnssv747377, nssv747378, nssv747379
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550733
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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