A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598966



Internal ID16386375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97605139..97760338hg38UCSC Ensembl
Innerchr5:96940843..97096042hg19UCSC Ensembl
Innerchr5:96966599..97121798hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38155200
hg19155200
hg18155200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9937n54
Supporting Variantsnssv1038115
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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