A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571500



Internal ID16012223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13201071..13202308hg38UCSC Ensembl
Innerchr16:13294928..13296165hg19UCSC Ensembl
Innerchr16:13202429..13203666hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381238
hg191238
hg181238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4913n54
Supporting Variantsnssv852751, nssv852750
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571500
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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