A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066317



Internal ID19155536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58880590..58914315hg38UCSC Ensembl
Innerchr16:58914494..58948219hg19UCSC Ensembl
Innerchr16:57471995..57505720hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3833726
hg1933726
hg1833726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559363
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066317
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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