A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722609



Internal ID19020890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35540930hg38UCSC Ensembl
Innerchr16:34470704..34775301hg19UCSC Ensembl
Innerchr16:34328205..34632802hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38304598
hg19304598
hg18304598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066148
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)nssv3722609
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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