A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556946



Internal ID18508541
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 StatusS
Merged Variantsnsv1046349
Supporting Variants
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)nssv3556946
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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