A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066924



Internal ID18809455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87911850..87998507hg38UCSC Ensembl
Innerchr16:87945456..88032113hg19UCSC Ensembl
Innerchr16:86502957..86589614hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3886658
hg1986658
hg1886658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719122
Samples
Known GenesBANP, CA5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066924
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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