A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559946



Internal ID18511541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84029323..84233403hg38UCSC Ensembl
Innerchr16:84062928..84267009hg19UCSC Ensembl
Innerchr16:82620429..82824510hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38204081
hg19204082
hg18204082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059227
Supporting Variants
Samples
Known GenesADAD2, DNAAF1, HSDL1, KCNG4, MBTPS1, SLC38A8, TAF1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559946
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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