A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597637



Internal ID16385046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26118200..26187756hg38UCSC Ensembl
Innerchr5:26118309..26187865hg19UCSC Ensembl
Innerchr5:26154066..26223622hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3869557
hg1969557
hg1869557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1028056, nssv1028057
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597637
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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