A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550749



Internal ID15991472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46306785hg38UCSC Ensembl
Innerchr10:47543322..47678021hg19UCSC Ensembl
Innerchr10:47013328..47148027hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38134700
hg19134700
hg18134700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n54
Supporting Variantsnssv1173602
SamplesHGDP00787
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550749
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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