A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556010



Internal ID18854291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34962968..35199952hg38UCSC Ensembl
Innerchr16:34197339..34434323hg19UCSC Ensembl
Innerchr16:34054840..34291824hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38236985
hg19236985
hg18236985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066136
Supporting Variants
Samples
Known GenesUBE2MP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556010
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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