A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064567



Internal ID19153786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35505629hg38UCSC Ensembl
Innerchr16:34470704..34740000hg19UCSC Ensembl
Innerchr16:34328205..34597501hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38269297
hg19269297
hg18269297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558403, nssv3558406, nssv3558409, nssv3722474, nssv3558408, nssv3558413, nssv3558410, nssv3558407, nssv3558422, nssv3558424, nssv3558423, nssv3722476, nssv3558416, nssv3558411, nssv3722478, nssv3722475, nssv3558419, nssv3558417, nssv3722477, nssv3558404, nssv3722480, nssv3722479, nssv3558412, nssv3558421, nssv3558405, nssv3558418, nssv3558414, nssv3558415, nssv3558420
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)nsv1064567
Frequency
Sample Size11257
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer