A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597818



Internal ID16385227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36440838..36460360hg38UCSC Ensembl
Innerchr5:36440940..36460462hg19UCSC Ensembl
Innerchr5:36476697..36496219hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3819523
hg1919523
hg1819523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9721n54
Supporting Variantsnssv1028955
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597818
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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