A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550757



Internal ID16338166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46332710hg38UCSC Ensembl
Innerchr10:47543322..47703946hg19UCSC Ensembl
Innerchr10:47013328..47173952hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38160625
hg19160625
hg18160625
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112n54
Supporting Variantsnssv747530, nssv747528, nssv747529, nssv747527
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550757
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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