A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057147



Internal ID18799678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77892138..77942626hg38UCSC Ensembl
Innerchr16:77926035..77976523hg19UCSC Ensembl
Innerchr16:76483536..76534024hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3850489
hg1950489
hg1850489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559670
Samples
Known GenesVAT1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057147
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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