A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046349



Internal ID18788880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:819378..942590hg38UCSC Ensembl
Innerchr16:869378..992590hg19UCSC Ensembl
Innerchr16:809379..932591hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38123213
hg19123213
hg18123213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556946
Samples
Known GenesLMF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046349
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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