A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571178



Internal ID16011901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1919082..1961125hg38UCSC Ensembl
Innerchr16:1969083..2011126hg19UCSC Ensembl
Innerchr16:1909084..1951127hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3842044
hg1942044
hg1842044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852073
Samples
Known GenesMSRB1, NDUFB10, RPL3L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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