A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573776



Internal ID16014499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830345..89831313hg38UCSC Ensembl
Innerchr16:89896753..89897721hg19UCSC Ensembl
Innerchr16:88424254..88425222hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38969
hg19969
hg18969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5328n54
Supporting Variantsnssv863543, nssv863545, nssv863546, nssv863544
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573776
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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