A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571200



Internal ID16011923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2209190..2244889hg38UCSC Ensembl
Innerchr16:2259191..2294890hg19UCSC Ensembl
Innerchr16:2199192..2234891hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3835700
hg1935700
hg1835700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852091
Samples
Known GenesBRICD5, DNASE1L2, E4F1, ECI1, MLST8, PGP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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