A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559251



Internal ID18857532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49127048..49175752hg38UCSC Ensembl
Innerchr16:49160959..49209663hg19UCSC Ensembl
Innerchr16:47718460..47767164hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3848705
hg1948705
hg1848705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066442
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559251
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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