A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572980



Internal ID16360389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75471148..75515987hg38UCSC Ensembl
Innerchr16:75505046..75549885hg19UCSC Ensembl
Innerchr16:74062547..74107386hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3844840
hg1944840
hg1844840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859181
Samples
Known GenesCHST6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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