A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598969



Internal ID16386378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97669437..97772855hg38UCSC Ensembl
Innerchr5:97005141..97108559hg19UCSC Ensembl
Innerchr5:97030897..97134315hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38103419
hg19103419
hg18103419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9938n54
Supporting Variantsnssv1038119, nssv1153053, nssv1038118
SamplesHGDP01399
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598969
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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