A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722521



Internal ID19020802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35521183hg38UCSC Ensembl
Innerchr16:34470704..34755554hg19UCSC Ensembl
Innerchr16:34328205..34613055hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38284851
hg19284851
hg18284851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062346
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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