A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066781



Internal ID19156000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35533904hg38UCSC Ensembl
Innerchr16:34466559..34768275hg19UCSC Ensembl
Innerchr16:34324060..34625776hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38301717
hg19301717
hg18301717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558360, nssv3722463, nssv3722460, nssv3558362, nssv3558353, nssv3558356, nssv3722461, nssv3722464, nssv3722462, nssv3558361, nssv3558358, nssv3558354, nssv3558355, nssv3558357, nssv3558359, nssv3722465
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)nsv1066781
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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