A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550735



Internal ID15991458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46370665hg38UCSC Ensembl
Innerchr10:47537368..47741882hg19UCSC Ensembl
Innerchr10:47007374..47211888hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38204534
hg19204515
hg18204515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1110n54
Supporting Variantsnssv747387, nssv747391, nssv747388, nssv747392, nssv747389, nssv747390, nssv747386
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550735
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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