A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149280



Internal ID15528177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:760039..797743hg38UCSC Ensembl
Innerchr16:810039..847743hg19UCSC Ensembl
Innerchr16:750040..787744hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837705
hg1937705
hg1837705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571024
Supporting Variants
SamplesHGDP00602
Known GenesCHTF18, MIR662, MSLN, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149280
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