A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065085



Internal ID19154304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35245310..35526596hg38UCSC Ensembl
Innerchr16:34479681..34760967hg19UCSC Ensembl
Innerchr16:34337182..34618468hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38281287
hg19281287
hg18281287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558935, nssv3558930, nssv3558923, nssv3558932, nssv3558929, nssv3558934, nssv3558927, nssv3558928, nssv3558931, nssv3558926, nssv3558922, nssv3558933, nssv3558925, nssv3558936, nssv3558924
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)nsv1065085
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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