A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550727



Internal ID15991450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46385067..46489856hg38UCSC Ensembl
Innerchr10:47041592..47164700hg19UCSC Ensembl
Innerchr10:46461598..46584706hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38104790
hg19123109
hg18123109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1106n54
Supporting Variantsnssv747370
Samples
Known GenesANXA8, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550727
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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