A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550750



Internal ID15991473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46325178hg38UCSC Ensembl
Innerchr10:47543322..47696414hg19UCSC Ensembl
Innerchr10:47013328..47166420hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38153093
hg19153093
hg18153093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n54
Supporting Variantsnssv747424, nssv1173605, nssv1173604, nssv1173603
Samples1798860569_A, HGDP00134, HGDP00884
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550750
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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