A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148910



Internal ID15534561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4960912..5284683hg38UCSC Ensembl
Innerchr16:5010913..5334684hg19UCSC Ensembl
Innerchr16:4950914..5274685hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38323772
hg19323772
hg18323772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571303
Supporting Variants
SamplesNINDS_90
Known GenesALG1, C16orf89, FAM86A, NAGPA, NAGPA-AS1, SEC14L5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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