A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045428



Internal ID19134647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7731805..7785977hg38UCSC Ensembl
Innerchr16:7781807..7835979hg19UCSC Ensembl
Innerchr16:7721808..7775980hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3854173
hg1954173
hg1854173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2719n100
Supporting Variantsnssv3557089
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)nsv1045428
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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