A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549957



Internal ID16337366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9095411..9174993hg38UCSC Ensembl
Innerchr10:9137374..9216956hg19UCSC Ensembl
Innerchr10:9177380..9256962hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3879583
hg1979583
hg1879583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744000
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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