A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055141



Internal ID19144360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78831480..78845486hg38UCSC Ensembl
Innerchr16:78865377..78879383hg19UCSC Ensembl
Innerchr16:77422878..77436884hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3814007
hg1914007
hg1814007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3038n100
Supporting Variantsnssv3719072
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055141
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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