A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600027



Internal ID16040750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151411237..151412430hg38UCSC Ensembl
Innerchr5:150790798..150791991hg19UCSC Ensembl
Innerchr5:150770991..150772184hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10125n54
Supporting Variantsnssv1043701
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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