A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597264



Internal ID16384673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15674526..15719997hg38UCSC Ensembl
Innerchr5:15674635..15720106hg19UCSC Ensembl
Innerchr5:15727635..15773106hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3845472
hg1945472
hg1845472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9610n54
Supporting Variantsnssv1153528
Samples1780862347_A
Known GenesFBXL7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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