A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064089



Internal ID18806620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89363245..89390942hg38UCSC Ensembl
Innerchr16:89429653..89457350hg19UCSC Ensembl
Innerchr16:87957154..87984851hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3827698
hg1927698
hg1827698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560005
Samples
Known GenesANKRD11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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