A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571504



Internal ID16012227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13201705..13202426hg38UCSC Ensembl
Innerchr16:13295562..13296283hg19UCSC Ensembl
Innerchr16:13203063..13203784hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38722
hg19722
hg18722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4915n54
Supporting Variantsnssv852773, nssv852769, nssv852772, nssv852771, nssv852770
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571504
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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