A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600885



Internal ID16388294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5424529..5454928hg38UCSC Ensembl
Innerchr6:5424762..5455161hg19UCSC Ensembl
Innerchr6:5369761..5400160hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3830400
hg1930400
hg1830400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1048754
Samples
Known GenesFARS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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