A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573775



Internal ID16014498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830345..89831255hg38UCSC Ensembl
Innerchr16:89896753..89897663hg19UCSC Ensembl
Innerchr16:88424254..88425164hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5328n54
Supporting Variantsnssv863542, nssv863540, nssv863541
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573775
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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