A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598646



Internal ID16386055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73447273..73448196hg38UCSC Ensembl
Innerchr5:72743100..72744021hg19UCSC Ensembl
Innerchr5:72778856..72779777hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38924
hg19922
hg18922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9878n54
Supporting Variantsnssv1035087
Samples
Known GenesFOXD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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