A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597871



Internal ID16038594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:39105492..39123914hg38UCSC Ensembl
Innerchr5:39105594..39124016hg19UCSC Ensembl
Innerchr5:39141351..39159773hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3818423
hg1918423
hg1818423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1029130
Samples
Known GenesFYB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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