A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571439



Internal ID16358848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9557668..9650238hg38UCSC Ensembl
Innerchr16:9651525..9744095hg19UCSC Ensembl
Innerchr16:9559026..9651596hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3892571
hg1992571
hg1892571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852518
Samples
Known GenesMIR7641-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571439
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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