A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996171



Internal ID15235031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:84166395..87066394hg38UCSC Ensembl
Outerchr16:84200001..87100000hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382900000
hg192900000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483044
Supporting Variants
Samples
Known GenesADAD2, ATP2C2, C16orf74, COTL1, COX4I1, CRISPLD2, DNAAF1, EMC8, FAM92B, FENDRR, FLJ30679, FOXC2, FOXF1, FOXL1, GINS2, GSE1, IRF8, KCNG4, KIAA0513, KLHL36, LINC00311, LINC00917, LINC01081, LINC01082, LOC146513, LOC400548, MIR1910, MIR5093, MIR6774, MIR7851, MTHFSD, TAF1C, TLDC1, USP10, WFDC1, ZDHHC7
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996171
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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