A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573360



Internal ID16360769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81492032..81545828hg38UCSC Ensembl
Innerchr16:81525637..81579433hg19UCSC Ensembl
Innerchr16:80083138..80136934hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3853797
hg1953797
hg1853797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149321
Samples1780862304_A
Known GenesCMIP, MIR7854
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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