A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054151



Internal ID19143370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11379565..11424919hg38UCSC Ensembl
Innerchr16:11473422..11518775hg19UCSC Ensembl
Innerchr16:11380923..11426276hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3845355
hg1945354
hg1845354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557136
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)nsv1054151
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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