A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719014



Internal ID19017295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70117612..70220744hg38UCSC Ensembl
Innerchr16:70151515..70254647hg19UCSC Ensembl
Innerchr16:68709016..68812148hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38103133
hg19103133
hg18103133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058420
Supporting Variants
Samples
Known GenesCLEC18C, LOC100506060, PDPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719014
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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