A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056426



Internal ID18798957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70048311..70118407hg38UCSC Ensembl
Innerchr16:70082214..70152310hg19UCSC Ensembl
Innerchr16:68639715..68709811hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3870097
hg1970097
hg1870097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3008n100
Supporting Variantsnssv3559516
Samples
Known GenesPDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056426
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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