A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066325



Internal ID19155544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33952512..34208804hg38UCSC Ensembl
Innerchr16:33754979..34011271hg19UCSC Ensembl
Innerchr16:33662480..33918772hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38256293
hg19256293
hg18256293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2958n100
Supporting Variantsnssv3555952, nssv3555950, nssv3555951, nssv3555949
Samples
Known GenesLINC00273
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066325
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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