A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597049



Internal ID16384458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8703036..8752644hg38UCSC Ensembl
Innerchr5:8703148..8752756hg19UCSC Ensembl
Innerchr5:8756148..8805756hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3849609
hg1949609
hg1849609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9568n54
Supporting Variantsnssv1024088, nssv1024087
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597049
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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