A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600286



Internal ID16387695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172616994..172652886hg38UCSC Ensembl
Innerchr5:172043997..172079889hg19UCSC Ensembl
Innerchr5:171976602..172012494hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3835893
hg1935893
hg1835893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10172n54
Supporting Variantsnssv1153123
SamplesHGDP01154
Known GenesNEURL1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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