A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549870



Internal ID16337279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4666435..4673284hg38UCSC Ensembl
Innerchr10:4708627..4715476hg19UCSC Ensembl
Innerchr10:4698627..4705476hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg386850
hg196850
hg186850
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743327, nssv743328, nssv743330, nssv743329, nssv743332, nssv743331
Samples
Known GenesLINC00704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549870
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer