A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063304



Internal ID19152523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35252489..35522700hg38UCSC Ensembl
Innerchr16:34486860..34757071hg19UCSC Ensembl
Innerchr16:34344361..34614572hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38270212
hg19270212
hg18270212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558950, nssv3558951, nssv3558955, nssv3558948, nssv3558954, nssv3558957, nssv3558949, nssv3558956, nssv3558952, nssv3558953, nssv3722641
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)nsv1063304
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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