A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550793



Internal ID15991516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46239982..46332377hg38UCSC Ensembl
Innerchr10:47611218..47703613hg19UCSC Ensembl
Innerchr10:47081224..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3892396
hg1992396
hg1892396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1115n54
Supporting Variantsnssv747632, nssv1174536
Samples1780862564_A
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550793
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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