A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548152



Internal ID18499747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21584980..21775408hg38UCSC Ensembl
Innerchr16:21596301..21786729hg19UCSC Ensembl
Innerchr16:21503802..21694230hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38190429
hg19190429
hg18190429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052153
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3548152
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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