A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550721



Internal ID15991444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46621229..46779725hg38UCSC Ensembl
Innerchr10:46769902..46928388hg19UCSC Ensembl
Innerchr10:46189908..46348394hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158497
hg19158487
hg18158487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747364
Samples
Known GenesFAM35BP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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