A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559847



Internal ID18511442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82146152..83636829hg38UCSC Ensembl
Innerchr16:82179757..83670434hg19UCSC Ensembl
Innerchr16:80737258..82227935hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381490678
hg191490678
hg181490678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061288
Supporting Variants
Samples
Known GenesCDH13, MIR3182, MIR8058, MPHOSPH6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559847
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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