A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549956



Internal ID16337365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9039746..9068825hg38UCSC Ensembl
Innerchr10:9081709..9110788hg19UCSC Ensembl
Innerchr10:9121715..9150794hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829080
hg1929080
hg1829080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743999
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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